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Denver Splint Co.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K940798
SHIPPERT PRESSURE BANDAGE
September 28, 1994
K940133
THE EXPANDACELL EAR PACK
May 23, 1994
K935724
THE EXPANDACELL SINUS PACK
May 12, 1994
K922062
THE DENVER CAUTERY
January 12, 1993