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FDA 510(k)

COPPER KETTLE VAPORIZER PLUS

K-Number: K771150 · 1977-08-04

ApplicantAir Products & Chemicals, Inc.
Decision Date1977-08-04
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COPPER KETTLE VAPORIZER PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Air Products & Chemicals, Inc.. It received FDA 510(k) clearance on 1977-08-04 under 510(k) number K771150. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COPPER KETTLE VAPORIZER PLUS?

COPPER KETTLE VAPORIZER PLUS is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Air Products & Chemicals, Inc.. The 510(k) number is K771150.

When did COPPER KETTLE VAPORIZER PLUS receive FDA 510(k) clearance?

COPPER KETTLE VAPORIZER PLUS received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771150.

Who is the listed applicant for COPPER KETTLE VAPORIZER PLUS?

The FDA 510(k) record lists Air Products & Chemicals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COPPER KETTLE VAPORIZER PLUS?

The FDA product code for COPPER KETTLE VAPORIZER PLUS is CAD.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Air Products & Chemicals, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K771134ANESTHESIA BREATHING CIRCUIT

Related Devices (Code: CAD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K240375V80 Anesthetic Vaporizer (V80)Shenzhen Mindray Bio-Medical Electronics Co., Ltd.K172702Tec 820, Tec 850Datex-Ohmeda, Inc.K110608SEVOFLURANE VAPORIZER ADAPTORPiramal Critcal Care, Inc (Formerly Minrad, Inc)K060331SIGMA ALPHA VAPORIZERPenlon LimitedK053564KEYED FILLER BOTTLE ADAPTOR, MODELS 53450, 53452, 53453, 53454Penlon LimitedK051666GAV - GENERAL ANAESTHETIC VAPORIZERGeneral Anaesthetic Services Limited

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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