Schneider-Shilley (Usa)

FDA Regulatory Profile

Schneider-Shilley (Usa) appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 24, 1989.

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K882826SOFTRAC-PTA PERIPHERAL DILATATION CATHETERJanuary 24, 1989
K875175MODIFIED PERIPHERAL DILATATION CATHETERSJuly 28, 1988
K881197SOFTRAC-PTA(TM) PERIPHERAL DILATATION CATHETERMay 16, 1988
K875323MODIFIED SCHNEIDER-SHILEY WIRE TORQUERMarch 28, 1988
K875322MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETERMarch 28, 1988
K875327MODIFIED SELDINGER INITIAL PUNCTURE INSTRUMENTMarch 25, 1988
K875324MODIFIED SCHNEIDER SHILEY INFLATION SYRINGESMarch 25, 1988
K875326MODIFIED SCHNEIDER-SHILEY FLUSHING CATHETERFebruary 18, 1988
K875325MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCKFebruary 18, 1988