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FDA 510(k)

PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER

K-Number: K874877 · 1988-02-22

ApplicantPegasus Airwave, Inc.
Decision Date1988-02-22
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER is the device name listed in this FDA 510(k) record. The listed applicant is Pegasus Airwave, Inc.. It received FDA 510(k) clearance on 1988-02-22 under 510(k) number K874877. 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 PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER?

PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER is a medical device that received FDA 510(k) clearance on 1988-02-22. The listed applicant is Pegasus Airwave, Inc.. The 510(k) number is K874877.

When did PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER receive FDA 510(k) clearance?

PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER received FDA 510(k) clearance on 1988-02-22, under 510(k) number K874877.

Who is the listed applicant for PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER?

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

What is the FDA product code for PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER?

The FDA product code for PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER 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 Pegasus Airwave, 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.

K944310PEGASUS BIWAVE PLUS SYSTEMK930742PEGASUS PROACTIVE WHEELCHAIR CUSHIONK933004PEGASUS BIWAVE SYSTEM

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

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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