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FDA 510(k)

KINETIC MOTION BED

K-Number: K823095 · 1982-12-03

ApplicantMotion Manufacturers, Inc.
Decision Date1982-12-03
Product CodeIKZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KINETIC MOTION BED is the device name listed in this FDA 510(k) record. The listed applicant is Motion Manufacturers, Inc.. It received FDA 510(k) clearance on 1982-12-03 under 510(k) number K823095. 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 KINETIC MOTION BED?

KINETIC MOTION BED is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Motion Manufacturers, Inc.. The 510(k) number is K823095.

When did KINETIC MOTION BED receive FDA 510(k) clearance?

KINETIC MOTION BED received FDA 510(k) clearance on 1982-12-03, under 510(k) number K823095.

Who is the listed applicant for KINETIC MOTION BED?

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

What is the FDA product code for KINETIC MOTION BED?

The FDA product code for KINETIC MOTION BED 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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