Last synced on 14 November 2025 at 11:06 pm

AMO PROFINESSE III ULTRASONIC HANDPIECE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K951462
510(k) Type
Traditional
Applicant
ALLERGAN MEDICAL OPTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1995
Days to Decision
77 days
Submission Type
Summary

AMO PROFINESSE III ULTRASONIC HANDPIECE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K951462
510(k) Type
Traditional
Applicant
ALLERGAN MEDICAL OPTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1995
Days to Decision
77 days
Submission Type
Summary