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FDA 510(k)

CHEST BELLOWS, SMALL

K-Number: K772367 · 1978-01-11

ApplicantHoneywell, Inc.
Decision Date1978-01-11
Product CodeCCM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CHEST BELLOWS, SMALL is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1978-01-11 under 510(k) number K772367. The device is classified under product code CCM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEST BELLOWS, SMALL?

CHEST BELLOWS, SMALL is a medical device that received FDA 510(k) clearance on 1978-01-11. The listed applicant is Honeywell, Inc.. The 510(k) number is K772367.

When did CHEST BELLOWS, SMALL receive FDA 510(k) clearance?

CHEST BELLOWS, SMALL received FDA 510(k) clearance on 1978-01-11, under 510(k) number K772367.

Who is the listed applicant for CHEST BELLOWS, SMALL?

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

What is the FDA product code for CHEST BELLOWS, SMALL?

The FDA product code for CHEST BELLOWS, SMALL is CCM.

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Other records listing Honeywell, Inc. as applicant

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Related Devices (Code: CCM)

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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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