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FDA 510(k)

ACTIVAPATCH

K-Number: K091326 · 2009-05-27

ApplicantActivatek, Inc.
Decision Date2009-05-27
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ACTIVAPATCH is the device name listed in this FDA 510(k) record. The listed applicant is Activatek, Inc.. It received FDA 510(k) clearance on 2009-05-27 under 510(k) number K091326. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTIVAPATCH?

ACTIVAPATCH is a medical device that received FDA 510(k) clearance on 2009-05-27. The listed applicant is Activatek, Inc.. The 510(k) number is K091326.

When did ACTIVAPATCH receive FDA 510(k) clearance?

ACTIVAPATCH received FDA 510(k) clearance on 2009-05-27, under 510(k) number K091326.

Who is the listed applicant for ACTIVAPATCH?

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

What is the FDA product code for ACTIVAPATCH?

The FDA product code for ACTIVAPATCH is EGJ.

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Other records listing Activatek, Inc. as applicant

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.

K061522TRIVARION BUFFERED IONTOPHORESIS ELECTRODE SYSTEM

Related Devices (Code: EGJ)

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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