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FDA 510(k)

NOVA AIR FLOATATION SYSTEM

K-Number: K780502 · 1978-04-10

ApplicantNova Health Systems, Inc.
Decision Date1978-04-10
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NOVA AIR FLOATATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nova Health Systems, Inc.. It received FDA 510(k) clearance on 1978-04-10 under 510(k) number K780502. 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 NOVA AIR FLOATATION SYSTEM?

NOVA AIR FLOATATION SYSTEM is a medical device that received FDA 510(k) clearance on 1978-04-10. The listed applicant is Nova Health Systems, Inc.. The 510(k) number is K780502.

When did NOVA AIR FLOATATION SYSTEM receive FDA 510(k) clearance?

NOVA AIR FLOATATION SYSTEM received FDA 510(k) clearance on 1978-04-10, under 510(k) number K780502.

Who is the listed applicant for NOVA AIR FLOATATION SYSTEM?

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

What is the FDA product code for NOVA AIR FLOATATION SYSTEM?

The FDA product code for NOVA AIR FLOATATION 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 Nova Health Systems, 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.

K895477NOVA PILLOWK893713NOVA OXYGEN TENT

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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