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FDA 510(k)

REST MATTRESS

K-Number: K971568 · 1997-07-18

ApplicantRest Mattress
Decision Date1997-07-18
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

REST MATTRESS is the device name listed in this FDA 510(k) record. The listed applicant is Rest Mattress. It received FDA 510(k) clearance on 1997-07-18 under 510(k) number K971568. 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 REST MATTRESS?

REST MATTRESS is a medical device that received FDA 510(k) clearance on 1997-07-18. The listed applicant is Rest Mattress. The 510(k) number is K971568.

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

REST MATTRESS received FDA 510(k) clearance on 1997-07-18, under 510(k) number K971568.

Who is the listed applicant for REST MATTRESS?

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

What is the FDA product code for REST MATTRESS?

The FDA product code for REST 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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