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FDA 510(k)

INTERMITTENT PRESSURE PAD

K-Number: K761227 · 1976-12-14

ApplicantFlowtron-Aire , Ltd.
Decision Date1976-12-14
Product Code
DecisionSubstantially Equivalent

Device Summary

INTERMITTENT PRESSURE PAD is the device name listed in this FDA 510(k) record. The listed applicant is Flowtron-Aire , Ltd.. It received FDA 510(k) clearance on 1976-12-14 under 510(k) number K761227. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERMITTENT PRESSURE PAD?

INTERMITTENT PRESSURE PAD is a medical device that received FDA 510(k) clearance on 1976-12-14. The listed applicant is Flowtron-Aire , Ltd.. The 510(k) number is K761227.

When did INTERMITTENT PRESSURE PAD receive FDA 510(k) clearance?

INTERMITTENT PRESSURE PAD received FDA 510(k) clearance on 1976-12-14, under 510(k) number K761227.

Who is the listed applicant for INTERMITTENT PRESSURE PAD?

The FDA 510(k) record lists Flowtron-Aire , Ltd. as the applicant. This does not by itself establish the device manufacturer.

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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