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Kappler, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K932738
KAPPLER PRO/VENT BOOT
March 29, 1994
K932694
KAPPLER PRO/VENT PROCEDURE GOWN
March 29, 1994