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FDA 510(k)

ABCO/GRANT ALTERNATING PRESSURE PAD & UT

K-Number: K800231 · 1980-02-26

ApplicantAbco Dealers, Inc.
Decision Date1980-02-26
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ABCO/GRANT ALTERNATING PRESSURE PAD & UT is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1980-02-26 under 510(k) number K800231. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABCO/GRANT ALTERNATING PRESSURE PAD & UT?

ABCO/GRANT ALTERNATING PRESSURE PAD & UT is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K800231.

When did ABCO/GRANT ALTERNATING PRESSURE PAD & UT receive FDA 510(k) clearance?

ABCO/GRANT ALTERNATING PRESSURE PAD & UT received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800231.

Who is the listed applicant for ABCO/GRANT ALTERNATING PRESSURE PAD & UT?

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

What is the FDA product code for ABCO/GRANT ALTERNATING PRESSURE PAD & UT?

The FDA product code for ABCO/GRANT ALTERNATING PRESSURE PAD & UT is FNM.

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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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