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FDA 510(k)

ULTRAFLOTATION MEDICAL WHEELCHAIR

K-Number: K884908 · 1988-12-27

Decision Date1988-12-27
Product CodeINF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ULTRAFLOTATION MEDICAL WHEELCHAIR 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 1988-12-27 under 510(k) number K884908. The device is classified under product code INF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRAFLOTATION MEDICAL WHEELCHAIR?

ULTRAFLOTATION MEDICAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1988-12-27. The listed applicant is Medical Flotation Systems, Inc.. The 510(k) number is K884908.

When did ULTRAFLOTATION MEDICAL WHEELCHAIR receive FDA 510(k) clearance?

ULTRAFLOTATION MEDICAL WHEELCHAIR received FDA 510(k) clearance on 1988-12-27, under 510(k) number K884908.

Who is the listed applicant for ULTRAFLOTATION MEDICAL WHEELCHAIR?

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 ULTRAFLOTATION MEDICAL WHEELCHAIR?

The FDA product code for ULTRAFLOTATION MEDICAL WHEELCHAIR is INF.

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: INF)

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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