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FDA 510(k)

SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEM

K-Number: K970081 · 1997-11-07

ApplicantCathay Consolidated, Inc.
Decision Date1997-11-07
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cathay Consolidated, Inc.. It received FDA 510(k) clearance on 1997-11-07 under 510(k) number K970081. 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 SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEM?

SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEM is a medical device that received FDA 510(k) clearance on 1997-11-07. The listed applicant is Cathay Consolidated, Inc.. The 510(k) number is K970081.

When did SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEM receive FDA 510(k) clearance?

SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEM received FDA 510(k) clearance on 1997-11-07, under 510(k) number K970081.

Who is the listed applicant for SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEM?

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

What is the FDA product code for SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEM?

The FDA product code for SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEM is FNM.

Related Clinical Trials

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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Other records listing Cathay Consolidated, Inc. as applicant

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.

K850626CARNATION OXYGEN

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.K955243BARIAIRKinetic Concepts, Inc.

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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