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FDA 510(k)

PEGASUS MATTRESS

K-Number: K833964 · 1984-01-30

ApplicantDermalex Co.
Decision Date1984-01-30
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PEGASUS MATTRESS is the device name listed in this FDA 510(k) record. The listed applicant is Dermalex Co.. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K833964. 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 MATTRESS?

PEGASUS MATTRESS is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Dermalex Co.. The 510(k) number is K833964.

When did PEGASUS MATTRESS receive FDA 510(k) clearance?

PEGASUS MATTRESS received FDA 510(k) clearance on 1984-01-30, under 510(k) number K833964.

Who is the listed applicant for PEGASUS MATTRESS?

The FDA 510(k) record lists Dermalex Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PEGASUS MATTRESS?

The FDA product code for PEGASUS MATTRESS 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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