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FDA 510(k)

MUFFLER, AIR PUMP

K-Number: K770392 · 1977-03-07

ApplicantCutter Laboratories, Inc.
Decision Date1977-03-07
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MUFFLER, AIR PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1977-03-07 under 510(k) number K770392. 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 MUFFLER, AIR PUMP?

MUFFLER, AIR PUMP is a medical device that received FDA 510(k) clearance on 1977-03-07. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K770392.

When did MUFFLER, AIR PUMP receive FDA 510(k) clearance?

MUFFLER, AIR PUMP received FDA 510(k) clearance on 1977-03-07, under 510(k) number K770392.

Who is the listed applicant for MUFFLER, AIR PUMP?

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

What is the FDA product code for MUFFLER, AIR PUMP?

The FDA product code for MUFFLER, AIR PUMP is 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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