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FDA 510(k)

TURNSOFT MATTRESS

K-Number: K913933 · 1992-01-10

ApplicantTurnsoft, Inc.
Decision Date1992-01-10
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TURNSOFT MATTRESS is the device name listed in this FDA 510(k) record. The listed applicant is Turnsoft, Inc.. It received FDA 510(k) clearance on 1992-01-10 under 510(k) number K913933. 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 TURNSOFT MATTRESS?

TURNSOFT MATTRESS is a medical device that received FDA 510(k) clearance on 1992-01-10. The listed applicant is Turnsoft, Inc.. The 510(k) number is K913933.

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

TURNSOFT MATTRESS received FDA 510(k) clearance on 1992-01-10, under 510(k) number K913933.

Who is the listed applicant for TURNSOFT MATTRESS?

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

What is the FDA product code for TURNSOFT MATTRESS?

The FDA product code for TURNSOFT MATTRESS 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Turnsoft, 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.

K923173OBALON COVER

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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