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Precision Instruments, Inc.

FDA Regulatory Profile

Precision Instruments, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 20, 1987.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K864520BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRONJanuary 20, 1987
K860648BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIAMarch 25, 1986
K843048RING SUPPORTED TREPHINE FOR CORNEA TRANSOctober 5, 1984
K801585HESSBURG-BFRRON TREPHINEOctober 3, 1980

FDA data resources