Last synced on 25 January 2026 at 3:41 am

ULTRASONIC PACHYMETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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