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FDA 510(k)

STAGE IV, CM-4000,MATTRESS OVERLAY SYSTEM

K-Number: K933091 · 1993-12-21

ApplicantCreative Medical, Inc.
Decision Date1993-12-21
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STAGE IV, CM-4000,MATTRESS OVERLAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Creative Medical, Inc.. It received FDA 510(k) clearance on 1993-12-21 under 510(k) number K933091. 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 STAGE IV, CM-4000,MATTRESS OVERLAY SYSTEM?

STAGE IV, CM-4000,MATTRESS OVERLAY SYSTEM is a medical device that received FDA 510(k) clearance on 1993-12-21. The listed applicant is Creative Medical, Inc.. The 510(k) number is K933091.

When did STAGE IV, CM-4000,MATTRESS OVERLAY SYSTEM receive FDA 510(k) clearance?

STAGE IV, CM-4000,MATTRESS OVERLAY SYSTEM received FDA 510(k) clearance on 1993-12-21, under 510(k) number K933091.

Who is the listed applicant for STAGE IV, CM-4000,MATTRESS OVERLAY SYSTEM?

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

What is the FDA product code for STAGE IV, CM-4000,MATTRESS OVERLAY SYSTEM?

The FDA product code for STAGE IV, CM-4000,MATTRESS OVERLAY SYSTEM is FNM.

Related Clinical Trials

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Other records listing Creative Medical, 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.

K852654CARDIAC COMMUNICATOR 2000

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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