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FDA 510(k)

MICROAIR PUP

K-Number: K925694 · 1993-03-24

ApplicantGsi Medical Systems
Decision Date1993-03-24
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MICROAIR PUP is the device name listed in this FDA 510(k) record. The listed applicant is Gsi Medical Systems. It received FDA 510(k) clearance on 1993-03-24 under 510(k) number K925694. The device is classified under product code IOQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROAIR PUP?

MICROAIR PUP is a medical device that received FDA 510(k) clearance on 1993-03-24. The listed applicant is Gsi Medical Systems. The 510(k) number is K925694.

When did MICROAIR PUP receive FDA 510(k) clearance?

MICROAIR PUP received FDA 510(k) clearance on 1993-03-24, under 510(k) number K925694.

Who is the listed applicant for MICROAIR PUP?

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

What is the FDA product code for MICROAIR PUP?

The FDA product code for MICROAIR PUP is IOQ.

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Related Devices (Code: IOQ)

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.

K122473TOTALCARE SPOT TOTALCARE BARIATRIC TOTALCARE DUO TOATALCARE BED SYSTEM TOTALCARE DUO2Hill-RomK973624NURSE'S AID PATIENT ROTATION SYSTEMAir Med Assist ProductsK970364AIRTEC2 LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970363HYDROTEC LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970636TOTALCARE., MODULAR THERAPY SYSTEM (MTS)Hill-Rom, Inc.K964873SILKAIR LOW AIRLOSS THERAPYHill-Rom, 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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