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FDA 510(k)

FLOTATION THERAPY BED

K-Number: K771264 · 1977-08-02

Decision Date1977-08-02
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FLOTATION THERAPY BED is the device name listed in this FDA 510(k) record. The listed applicant is Aquarius Medical Services. It received FDA 510(k) clearance on 1977-08-02 under 510(k) number K771264. 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 FLOTATION THERAPY BED?

FLOTATION THERAPY BED is a medical device that received FDA 510(k) clearance on 1977-08-02. The listed applicant is Aquarius Medical Services. The 510(k) number is K771264.

When did FLOTATION THERAPY BED receive FDA 510(k) clearance?

FLOTATION THERAPY BED received FDA 510(k) clearance on 1977-08-02, under 510(k) number K771264.

Who is the listed applicant for FLOTATION THERAPY BED?

The FDA 510(k) record lists Aquarius Medical Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOTATION THERAPY BED?

The FDA product code for FLOTATION THERAPY 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.

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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