FDA 510(k)

PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM

K-Number: K872228 · 1987-09-04

Decision Date1987-09-04

Product CodeFNM

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1987-09-04 under 510(k) number K872228. 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 PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM?

PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM is a medical device that received FDA 510(k) clearance on 1987-09-04. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K872228.

When did PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM receive FDA 510(k) clearance?

PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM received FDA 510(k) clearance on 1987-09-04, under 510(k) number K872228.

Who is the listed applicant for PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM?

The FDA 510(k) record lists American Pharmaseal Div. Ahsc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM?

The FDA product code for PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM 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.