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FDA 510(k)

RESPIRATORY KIT

K-Number: K772047 · 1977-11-23

ApplicantAmerican Hospital Supply Corp.
Decision Date1977-11-23
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRATORY KIT is the device name listed in this FDA 510(k) record. The listed applicant is American Hospital Supply Corp.. It received FDA 510(k) clearance on 1977-11-23 under 510(k) number K772047. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRATORY KIT?

RESPIRATORY KIT is a medical device that received FDA 510(k) clearance on 1977-11-23. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K772047.

When did RESPIRATORY KIT receive FDA 510(k) clearance?

RESPIRATORY KIT received FDA 510(k) clearance on 1977-11-23, under 510(k) number K772047.

Who is the listed applicant for RESPIRATORY KIT?

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

What is the FDA product code for RESPIRATORY KIT?

The FDA product code for RESPIRATORY KIT is CAH.

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Other records listing American Hospital Supply Corp. 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.

K854739AMERICAN STERILE SURGICAL ABSORBENT TOWELK854759AMERICAN STERILE MAYO STAND TRAYK832826AAP DOSIMETRY RELEASE OR BASIN SETSK830546DOSIMETRIC RELEASEK822990CONVERTORS PRIMARY WOUND DRESSING IIK830343CONTAINER W/PRIMING SOLUTION

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Related Devices (Code: CAH)

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Official Source

View on FDA Database →

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

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