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FDA 510(k)

PRO-2000 LOW AIR LOSS THERAPY BED

K-Number: K926403 · 1993-07-30

ApplicantCh Administration, Inc.
Decision Date1993-07-30
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRO-2000 LOW AIR LOSS THERAPY BED is the device name listed in this FDA 510(k) record. The listed applicant is Ch Administration, Inc.. It received FDA 510(k) clearance on 1993-07-30 under 510(k) number K926403. 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 PRO-2000 LOW AIR LOSS THERAPY BED?

PRO-2000 LOW AIR LOSS THERAPY BED is a medical device that received FDA 510(k) clearance on 1993-07-30. The listed applicant is Ch Administration, Inc.. The 510(k) number is K926403.

When did PRO-2000 LOW AIR LOSS THERAPY BED receive FDA 510(k) clearance?

PRO-2000 LOW AIR LOSS THERAPY BED received FDA 510(k) clearance on 1993-07-30, under 510(k) number K926403.

Who is the listed applicant for PRO-2000 LOW AIR LOSS THERAPY BED?

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

What is the FDA product code for PRO-2000 LOW AIR LOSS THERAPY BED?

The FDA product code for PRO-2000 LOW AIR LOSS THERAPY BED 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 Ch Administration, 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.

K953196CARDIO-SYSTEMS PRO-OPK926402COMFORT CARE LOW AIR LOSS THERAPY BED

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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