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FDA 510(k)

SINGLE AMPLIFIER FOR BOTOX

K-Number: K051852 · 2005-09-14

ApplicantAllergan, Inc.
Decision Date2005-09-14
Product CodeGWL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SINGLE AMPLIFIER FOR BOTOX is the device name listed in this FDA 510(k) record. The listed applicant is Allergan, Inc.. It received FDA 510(k) clearance on 2005-09-14 under 510(k) number K051852. The device is classified under product code GWL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINGLE AMPLIFIER FOR BOTOX?

SINGLE AMPLIFIER FOR BOTOX is a medical device that received FDA 510(k) clearance on 2005-09-14. The listed applicant is Allergan, Inc.. The 510(k) number is K051852.

When did SINGLE AMPLIFIER FOR BOTOX receive FDA 510(k) clearance?

SINGLE AMPLIFIER FOR BOTOX received FDA 510(k) clearance on 2005-09-14, under 510(k) number K051852.

Who is the listed applicant for SINGLE AMPLIFIER FOR BOTOX?

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

What is the FDA product code for SINGLE AMPLIFIER FOR BOTOX?

The FDA product code for SINGLE AMPLIFIER FOR BOTOX is GWL.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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