FDA 510(k)

LOW AIR LOSS BED

K-Number: K871705 · 1987-10-09

ApplicantIntegrated Medical Equipment Co.

Decision Date1987-10-09

Product CodeFNM

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

LOW AIR LOSS BED is the device name listed in this FDA 510(k) record. The listed applicant is Integrated Medical Equipment Co.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K871705. 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 LOW AIR LOSS BED?

LOW AIR LOSS BED is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Integrated Medical Equipment Co.. The 510(k) number is K871705.

When did LOW AIR LOSS BED receive FDA 510(k) clearance?

LOW AIR LOSS BED received FDA 510(k) clearance on 1987-10-09, under 510(k) number K871705.

Who is the listed applicant for LOW AIR LOSS BED?

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

What is the FDA product code for LOW AIR LOSS BED?

The FDA product code for LOW AIR LOSS BED is FNM.

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 Kansas K974070PHYSIO/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.