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FDA 510(k)

B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT

K-Number: K915671 · 1992-01-13

ApplicantProgressive Medical Technology, Inc.
Decision Date1992-01-13
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Medical Technology, Inc.. It received FDA 510(k) clearance on 1992-01-13 under 510(k) number K915671. 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 B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT?

B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT is a medical device that received FDA 510(k) clearance on 1992-01-13. The listed applicant is Progressive Medical Technology, Inc.. The 510(k) number is K915671.

When did B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT receive FDA 510(k) clearance?

B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT received FDA 510(k) clearance on 1992-01-13, under 510(k) number K915671.

Who is the listed applicant for B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT?

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

What is the FDA product code for B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT?

The FDA product code for B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT is IOQ.

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Other records listing Progressive Medical Technology, 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.

K923710OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BEDK915638TALLEY TM200 INTERMTTENT COMPRESSION UNITK915092TALLEY TM300 SEQUENTIAL MULTICOM COMPRESSION SYSTK915637TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST.

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 ProductsK970363HYDROTEC LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970364AIRTEC2 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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