FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SINGLE AMPLIFIER FOR BOTOX

K Number: K051852 · Decision Sep 14, 2005
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
52
Applicant Total
33
Review Days
68

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Basic Information

Device Name
SINGLE AMPLIFIER FOR BOTOX
K Number
K051852
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1835
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Allergan, Inc.
Date Received
July 8, 2005
Decision Date
September 14, 2005
Product Code
GWL
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWL Amplifier, Physiological Signal

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K014202 COMPLETE BRAND MULTI-PURPOSE SOLUTION
K013479 COMPLETE BRAND MULTI-PURPOSE SOLUTION
K003252 COMPLETE BRAND MULTI-PURPOSE SOLUTION
K003638 MOJAVE CATARACT EXTRACTION SYSTEM
K003109 COMPLETE BRAND LUBRICATING AND REWETTING DROPS
K000164 COMPLETE BRAND COMFORTPLUS MULTI-PURPOSE SOLUTION
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