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SINGLE AMPLIFIER FOR BOTOX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051852
510(k) Type
Traditional
Applicant
ALLERGAN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2005
Days to Decision
68 days
Submission Type
Statement

SINGLE AMPLIFIER FOR BOTOX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051852
510(k) Type
Traditional
Applicant
ALLERGAN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2005
Days to Decision
68 days
Submission Type
Statement