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Precise Medical Products

FDA Regulatory Profile

Precise Medical Products appears in FDA public data with 0 recalls, 2 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 16, 2006.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K061409SMARTINFUSER PAINPUMP, MODEL P49220 W/CATHETER SET; P49224N W/O CATHETER SETJune 16, 2006
K042122SMARTINFUSER PAINPUMPSeptember 22, 2004

FDA data resources