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FDA 510(k)

ALPHABED ALTERNATING PRESSURE PAD

K-Number: K761012 · 1976-12-09

ApplicantNlowtron-Aire , Ltd.
Decision Date1976-12-09
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALPHABED ALTERNATING PRESSURE PAD is the device name listed in this FDA 510(k) record. The listed applicant is Nlowtron-Aire , Ltd.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K761012. 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 ALPHABED ALTERNATING PRESSURE PAD?

ALPHABED ALTERNATING PRESSURE PAD is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Nlowtron-Aire , Ltd.. The 510(k) number is K761012.

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

ALPHABED ALTERNATING PRESSURE PAD received FDA 510(k) clearance on 1976-12-09, under 510(k) number K761012.

Who is the listed applicant for ALPHABED ALTERNATING PRESSURE PAD?

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

What is the FDA product code for ALPHABED ALTERNATING PRESSURE PAD?

The FDA product code for ALPHABED ALTERNATING PRESSURE PAD is FNM.

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Related Devices (Code: FNM)

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.

K973169PRESSURE GUARD SITE SELECT (A)Span-America Medical Systems, Inc.K972022ZAK-2000Cardio Systems, Inc.K974319MIGHTY AIRWheelchairs of KansasK974070PHYSIO/1000Physio Designs, Inc.K972549SIMPULSEKinetic Concepts, Inc.K970081SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEMCathay Consolidated, Inc.

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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