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FDA 510(k)

M.F.S. LOW AIR LOSS PULSATING BED

K-Number: K893801 · 1989-07-25

Decision Date1989-07-25
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

M.F.S. LOW AIR LOSS PULSATING BED is the device name listed in this FDA 510(k) record. The listed applicant is Medical Flotation Systems, Inc.. It received FDA 510(k) clearance on 1989-07-25 under 510(k) number K893801. 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 M.F.S. LOW AIR LOSS PULSATING BED?

M.F.S. LOW AIR LOSS PULSATING BED is a medical device that received FDA 510(k) clearance on 1989-07-25. The listed applicant is Medical Flotation Systems, Inc.. The 510(k) number is K893801.

When did M.F.S. LOW AIR LOSS PULSATING BED receive FDA 510(k) clearance?

M.F.S. LOW AIR LOSS PULSATING BED received FDA 510(k) clearance on 1989-07-25, under 510(k) number K893801.

Who is the listed applicant for M.F.S. LOW AIR LOSS PULSATING BED?

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

What is the FDA product code for M.F.S. LOW AIR LOSS PULSATING BED?

The FDA product code for M.F.S. LOW AIR LOSS PULSATING BED is IOQ.

Related Clinical Trials

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.

Other records listing Medical Flotation Systems, 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.

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.

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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