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Smith & Nephew Equipment Group

FDA Regulatory Profile

Smith & Nephew Equipment Group 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 April 2, 1991.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K910783SHAMPAINE MODEL 3800 OR MURANAKA MODEL OR-604MApril 2, 1991
K904965SHAMPAINE 1000 SERIES ANGENIEUX AX-14 DUO,AX-4January 16, 1991

FDA data resources