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FDA 510(k)

DRAGER-VAPOR 19.1

K-Number: K942055 · 1995-01-27

ApplicantNorth American Grager
Decision Date1995-01-27
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DRAGER-VAPOR 19.1 is the device name listed in this FDA 510(k) record. The listed applicant is North American Grager. It received FDA 510(k) clearance on 1995-01-27 under 510(k) number K942055. 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 DRAGER-VAPOR 19.1?

DRAGER-VAPOR 19.1 is a medical device that received FDA 510(k) clearance on 1995-01-27. The listed applicant is North American Grager. The 510(k) number is K942055.

When did DRAGER-VAPOR 19.1 receive FDA 510(k) clearance?

DRAGER-VAPOR 19.1 received FDA 510(k) clearance on 1995-01-27, under 510(k) number K942055.

Who is the listed applicant for DRAGER-VAPOR 19.1?

The FDA 510(k) record lists North American Grager as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRAGER-VAPOR 19.1?

The FDA product code for DRAGER-VAPOR 19.1 is CAD.

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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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