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FDA 510(k)

TURN EZ BED DEVICE

K-Number: K922473 · 1992-09-09

ApplicantMed-Ez, Inc.
Decision Date1992-09-09
Product CodeIKZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TURN EZ BED DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Med-Ez, Inc.. It received FDA 510(k) clearance on 1992-09-09 under 510(k) number K922473. 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 TURN EZ BED DEVICE?

TURN EZ BED DEVICE is a medical device that received FDA 510(k) clearance on 1992-09-09. The listed applicant is Med-Ez, Inc.. The 510(k) number is K922473.

When did TURN EZ BED DEVICE receive FDA 510(k) clearance?

TURN EZ BED DEVICE received FDA 510(k) clearance on 1992-09-09, under 510(k) number K922473.

Who is the listed applicant for TURN EZ BED DEVICE?

The FDA 510(k) record lists Med-Ez, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TURN EZ BED DEVICE?

The FDA product code for TURN EZ BED DEVICE is IKZ.

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Related Devices (Code: IKZ)

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.

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.

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