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Denver Splint Co.

FDA Regulatory Profile

Denver Splint Co. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 28, 1994.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K940798SHIPPERT PRESSURE BANDAGESeptember 28, 1994
K940133THE EXPANDACELL EAR PACKMay 23, 1994
K935724THE EXPANDACELL SINUS PACKMay 12, 1994
K922062THE DENVER CAUTERYJanuary 12, 1993

FDA data resources