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Anchor Products Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Known Names

anchor products company, anchor products

Recent 510(k) Clearances

K-NumberDeviceDate
K091930ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SBSeptember 23, 2009
K061555ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEMAugust 31, 2006
K982073ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEMSeptember 22, 1998
K884862ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADEDecember 27, 1988
K873124ANCHOR BIOPSY NEEDLESeptember 8, 1987
K831648ANCHOR BRAND SURGICAL NEEDLESAugust 16, 1983
K790405ANCHOR BRAND COUNT-TAINERMarch 26, 1979