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FDA 510(k)

MODEL CNA-1 VAPORIZER

K-Number: K761160 · 1976-12-09

Decision Date1976-12-09
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL CNA-1 VAPORIZER is the device name listed in this FDA 510(k) record. The listed applicant is Cyprane North America, Inc.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K761160. 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 MODEL CNA-1 VAPORIZER?

MODEL CNA-1 VAPORIZER is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Cyprane North America, Inc.. The 510(k) number is K761160.

When did MODEL CNA-1 VAPORIZER receive FDA 510(k) clearance?

MODEL CNA-1 VAPORIZER received FDA 510(k) clearance on 1976-12-09, under 510(k) number K761160.

Who is the listed applicant for MODEL CNA-1 VAPORIZER?

The FDA 510(k) record lists Cyprane North America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL CNA-1 VAPORIZER?

The FDA product code for MODEL CNA-1 VAPORIZER 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.

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.

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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