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FDA 510(k)

COMFORT CARE LOW AIR LOSS THERAPY BED

K-Number: K926402 · 1993-03-24

ApplicantCh Administration, Inc.
Decision Date1993-03-24
Product CodeINX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

COMFORT CARE 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 1993-03-24 under 510(k) number K926402. The device is classified under product code INX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMFORT CARE LOW AIR LOSS THERAPY BED?

COMFORT CARE LOW AIR LOSS THERAPY BED is a medical device that received FDA 510(k) clearance on 1993-03-24. The listed applicant is Ch Administration, Inc.. The 510(k) number is K926402.

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

COMFORT CARE LOW AIR LOSS THERAPY BED received FDA 510(k) clearance on 1993-03-24, under 510(k) number K926402.

Who is the listed applicant for COMFORT CARE 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 COMFORT CARE LOW AIR LOSS THERAPY BED?

The FDA product code for COMFORT CARE LOW AIR LOSS THERAPY BED is INX.

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-OPK926403PRO-2000 LOW AIR LOSS THERAPY BED

Related Devices (Code: INX)

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.

K972176HOME CARE BEAD BEDKinetic Concepts, Inc.K964223CLINITRON RITE-HITEHill-Rom, Inc.K943385CLINITRON ELEXISSsi Medical Services, Inc.K942184CLINITRON AT HOME AIR FLUIDED THERAPYSsi Medical Services, Inc.K931168X-20 AIR SUPPORT BEDAmerican Life Support Technology, Inc.K934689LOW AIR LOSS MATTRESS, MODIFICATIONCardio Systems, 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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