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FDA 510(k)

MICROAIR FLUIDIZED AIR BED

K-Number: K884529 · 1988-11-18

ApplicantGsi Development Co.
Decision Date1988-11-18
Product CodeINX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MICROAIR FLUIDIZED AIR BED is the device name listed in this FDA 510(k) record. The listed applicant is Gsi Development Co.. It received FDA 510(k) clearance on 1988-11-18 under 510(k) number K884529. 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 MICROAIR FLUIDIZED AIR BED?

MICROAIR FLUIDIZED AIR BED is a medical device that received FDA 510(k) clearance on 1988-11-18. The listed applicant is Gsi Development Co.. The 510(k) number is K884529.

When did MICROAIR FLUIDIZED AIR BED receive FDA 510(k) clearance?

MICROAIR FLUIDIZED AIR BED received FDA 510(k) clearance on 1988-11-18, under 510(k) number K884529.

Who is the listed applicant for MICROAIR FLUIDIZED AIR BED?

The FDA 510(k) record lists Gsi Development Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROAIR FLUIDIZED AIR BED?

The FDA product code for MICROAIR FLUIDIZED AIR 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 Gsi Development Co. 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.

K926456MICROAIR TURN-QK914674MICROAIR 3500K893708FLUIDIZED AIR 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

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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