FDA 510(k)

AQUA MED

K-Number: K914943 · 1992-04-02

Decision Date1992-04-02

Product CodeISA

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

AQUA MED is the device name listed in this FDA 510(k) record. The listed applicant is Aqua Massage Intl., Inc.. It received FDA 510(k) clearance on 1992-04-02 under 510(k) number K914943. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUA MED?

AQUA MED is a medical device that received FDA 510(k) clearance on 1992-04-02. The listed applicant is Aqua Massage Intl., Inc.. The 510(k) number is K914943.

When did AQUA MED receive FDA 510(k) clearance?

AQUA MED received FDA 510(k) clearance on 1992-04-02, under 510(k) number K914943.

Who is the listed applicant for AQUA MED?

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

What is the FDA product code for AQUA MED?

The FDA product code for AQUA MED is ISA.

Related Devices (Code: ISA)

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.