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Retrax

FDA Regulatory Profile

Retrax appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 26, 1993.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K920706MAGNETIC POINT GUARD FOR SURGICAL NEEDLESMay 26, 1993
K901508RETRAX SAFETY SYRINGEJune 14, 1990

FDA data resources