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FDA 510(k)

AQUA PATCH

K-Number: K973693 · 1997-12-18

ApplicantPci Technology
Decision Date1997-12-18
Product CodeMGQ
DecisionSubstantially Equivalent for Some Indications

Device Summary

AQUA PATCH is the device name listed in this FDA 510(k) record. The listed applicant is Pci Technology. It received FDA 510(k) clearance on 1997-12-18 under 510(k) number K973693. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the AQUA PATCH?

AQUA PATCH is a medical device that received FDA 510(k) clearance on 1997-12-18. The listed applicant is Pci Technology. The 510(k) number is K973693.

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

AQUA PATCH received FDA 510(k) clearance on 1997-12-18, under 510(k) number K973693.

Who is the listed applicant for AQUA PATCH?

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

What is the FDA product code for AQUA PATCH?

The FDA product code for AQUA PATCH is MGQ.

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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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