FDA 510(k)

MARK IV FLOATATION THERAPY BED

K-Number: K901890 · 1990-05-07

ApplicantHydrothermic Floatation Systems, Inc.

Decision Date1990-05-07

Product CodeIOQ

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

MARK IV FLOATATION THERAPY BED is the device name listed in this FDA 510(k) record. The listed applicant is Hydrothermic Floatation Systems, Inc.. It received FDA 510(k) clearance on 1990-05-07 under 510(k) number K901890. 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 MARK IV FLOATATION THERAPY BED?

MARK IV FLOATATION THERAPY BED is a medical device that received FDA 510(k) clearance on 1990-05-07. The listed applicant is Hydrothermic Floatation Systems, Inc.. The 510(k) number is K901890.

When did MARK IV FLOATATION THERAPY BED receive FDA 510(k) clearance?

MARK IV FLOATATION THERAPY BED received FDA 510(k) clearance on 1990-05-07, under 510(k) number K901890.

Who is the listed applicant for MARK IV FLOATATION THERAPY BED?

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

What is the FDA product code for MARK IV FLOATATION THERAPY BED?

The FDA product code for MARK IV FLOATATION THERAPY BED is IOQ.

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Related Devices (Code: IOQ)

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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.