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ULTRASONIC PACHYMETER

Page Type
Cleared 510(K)
510(k) Number
K921705
510(k) Type
Traditional
Applicant
PRECISION CORNEAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1992
Days to Decision
220 days
Submission Type
Statement

ULTRASONIC PACHYMETER

Page Type
Cleared 510(K)
510(k) Number
K921705
510(k) Type
Traditional
Applicant
PRECISION CORNEAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1992
Days to Decision
220 days
Submission Type
Statement