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AOI UNIVERSAL ULTRASONIC HANDPIECE

Page Type
Cleared 510(K)
510(k) Number
K950880
510(k) Type
Traditional
Applicant
AMERICAN OPTICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1995
Days to Decision
88 days
Submission Type
Summary

AOI UNIVERSAL ULTRASONIC HANDPIECE

Page Type
Cleared 510(K)
510(k) Number
K950880
510(k) Type
Traditional
Applicant
AMERICAN OPTICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1995
Days to Decision
88 days
Submission Type
Summary