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FDA 510(k)

GALAXY MD SERIES THERAPYPOOLS

K-Number: K945824 · 1995-04-05

ApplicantGalaxy Aquatics, Inc.
Decision Date1995-04-05
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GALAXY MD SERIES THERAPYPOOLS is the device name listed in this FDA 510(k) record. The listed applicant is Galaxy Aquatics, Inc.. It received FDA 510(k) clearance on 1995-04-05 under 510(k) number K945824. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GALAXY MD SERIES THERAPYPOOLS?

GALAXY MD SERIES THERAPYPOOLS is a medical device that received FDA 510(k) clearance on 1995-04-05. The listed applicant is Galaxy Aquatics, Inc.. The 510(k) number is K945824.

When did GALAXY MD SERIES THERAPYPOOLS receive FDA 510(k) clearance?

GALAXY MD SERIES THERAPYPOOLS received FDA 510(k) clearance on 1995-04-05, under 510(k) number K945824.

Who is the listed applicant for GALAXY MD SERIES THERAPYPOOLS?

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

What is the FDA product code for GALAXY MD SERIES THERAPYPOOLS?

The FDA product code for GALAXY MD SERIES THERAPYPOOLS is BXB.

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Related Devices (Code: BXB)

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.

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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.

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