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FDA 510(k)

MICOS MICROPULSE(TM) ALTERNATING PRESSURE MATTRESS

K-Number: K945629 · 1995-04-14

ApplicantMicos Medical Systems
Decision Date1995-04-14
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICOS MICROPULSE(TM) ALTERNATING PRESSURE MATTRESS is the device name listed in this FDA 510(k) record. The listed applicant is Micos Medical Systems. It received FDA 510(k) clearance on 1995-04-14 under 510(k) number K945629. 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 MICOS MICROPULSE(TM) ALTERNATING PRESSURE MATTRESS?

MICOS MICROPULSE(TM) ALTERNATING PRESSURE MATTRESS is a medical device that received FDA 510(k) clearance on 1995-04-14. The listed applicant is Micos Medical Systems. The 510(k) number is K945629.

When did MICOS MICROPULSE(TM) ALTERNATING PRESSURE MATTRESS receive FDA 510(k) clearance?

MICOS MICROPULSE(TM) ALTERNATING PRESSURE MATTRESS received FDA 510(k) clearance on 1995-04-14, under 510(k) number K945629.

Who is the listed applicant for MICOS MICROPULSE(TM) ALTERNATING PRESSURE MATTRESS?

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

What is the FDA product code for MICOS MICROPULSE(TM) ALTERNATING PRESSURE MATTRESS?

The FDA product code for MICOS MICROPULSE(TM) ALTERNATING PRESSURE 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 Micos Medical Systems 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.

K945845MICOS MICROPULSE(TM) OR TABLE PATIENT SUPPORTK945667MICOS MICROPULSE(TM) ALTERNATING PRESSURE WHEELCHAIR CUSHION

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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