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Anspach Mfg., Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K940276
FILTER, DIFFUSER
November 16, 1994
K925328
ANSPACH BONE RIVET, ANSPACH SUTURE ANCHOR
October 27, 1993
K905027
CUP OUT
February 5, 1991