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FDA 510(k)

CBG CUFF MANOMETER

K-Number: K873614 · 1988-01-22

ApplicantBio-Med Devices, Inc.
Decision Date1988-01-22
Product CodeBSK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CBG CUFF MANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Med Devices, Inc.. It received FDA 510(k) clearance on 1988-01-22 under 510(k) number K873614. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CBG CUFF MANOMETER?

CBG CUFF MANOMETER is a medical device that received FDA 510(k) clearance on 1988-01-22. The listed applicant is Bio-Med Devices, Inc.. The 510(k) number is K873614.

When did CBG CUFF MANOMETER receive FDA 510(k) clearance?

CBG CUFF MANOMETER received FDA 510(k) clearance on 1988-01-22, under 510(k) number K873614.

Who is the listed applicant for CBG CUFF MANOMETER?

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

What is the FDA product code for CBG CUFF MANOMETER?

The FDA product code for CBG CUFF MANOMETER is BSK.

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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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