42 U.S.C. § 7671 - Definitions
|Cite as:||42 U.S.C. § 7671|
|Currency:||Current through P.L. 116-158 (08/14/2020)|
As used in this subchapter-
The term "appliance" means any device which contains and uses a class I or class II substance as a refrigerant and which is used for household or commercial purposes, including any air conditioner, refrigerator, chiller, or freezer.
(2) Baseline year
The term "baseline year" means-
(A) the calendar year 1986, in the case of any class I substance listed in Group I or II under section 7671a(a) of this title,
(B) the calendar year 1989, in the case of any class I substance listed in Group III, IV, or V under section 7671a(a) of this title, and
(C) a representative calendar year selected by the Administrator, in the case of-
(i) any substance added to the list of class I substances after the publication of the initial list under section 7671a(a) of this title, and
(ii) any class II substance.
(3) Class I substance
The term "class I substance" means each of the substances listed as provided in section 7671a(a) of this title.
(4) Class II substance
The term "class II substance" means each of the substances listed as provided in section 7671a(b) of this title.
The term "Commissioner" means the Commissioner of the Food and Drug Administration.
The term "consumption" means, with respect to any substance, the amount of that substance produced in the United States, plus the amount imported, minus the amount exported to Parties to the Montreal Protocol. Such term shall be construed in a manner consistent with the Montreal Protocol.
The term "import" means to land on, bring into, or introduce into, or attempt to land on, bring into, or introduce into, any place subject to the jurisdiction of the United States, whether or not such landing, bringing, or introduction constitutes an importation within the meaning of the customs laws of the United States.
(8) Medical device
The term "medical device" means any device (as defined in the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 321 )), diagnostic product, drug (as defined in the Federal Food, Drug, and Cosmetic Act), and drug delivery system-
(A) if such device, product, drug, or drug delivery system utilizes a class I or class II substance for which no safe and effective alternative has been developed, and where necessary, approved by the Commissioner; and
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