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Tenet Medical Engineering

FDA Regulatory Profile

Tenet Medical Engineering appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 14, 1997.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K963505TENET MLTI-POSITIONING SURGICAL STIRRUP SYSTEMFebruary 14, 1997
K963506TENET RADIOLUCENT HAND TABLEJanuary 9, 1997
K964102TENET TIBIAL FRACTURE SUPPORTDecember 5, 1996

FDA data resources