FDA 510(k)

OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED

K-Number: K923710 · 1993-03-22

ApplicantProgressive Medical Technology, Inc.

Decision Date1993-03-22

Product CodeIKZ

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED 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 1993-03-22 under 510(k) number K923710. The device is classified under product code IKZ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED?

OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED is a medical device that received FDA 510(k) clearance on 1993-03-22. The listed applicant is Progressive Medical Technology, Inc.. The 510(k) number is K923710.

When did OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED receive FDA 510(k) clearance?

OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED received FDA 510(k) clearance on 1993-03-22, under 510(k) number K923710.

Who is the listed applicant for OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED?

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 OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED?

The FDA product code for OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED is IKZ.

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Other records listing Progressive Medical Technology, Inc. as applicant

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Related Devices (Code: IKZ)

K972486PRESSUREGUARD IVSpan-America Medical Systems, Inc.K972111RUMORS DYNAMIC AIR THERAPY UNITHill-Rom, Inc.K962788CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEMGaymar Industries, Inc.K954671THE FREEDOM BEDProbed Medical Technologies, Inc.K950756PULMONEX DYNAMIC AIR THERAPY UNITHill-Rom, Inc.K950681MODEL TURN Q PLUS AUTOMATIC TURNING MATTRESS WITH LOW AIR LOSS THERAPYInvacare Corp.

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.