Anchor Products Co.
Anchor Products Co. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 2009.
Top product codes for Anchor Products Co.
Recent clearances by Anchor Products Co.
- K091930 — ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SB
- K061555 — ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM
- K982073 — ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM
- K884862 — ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE
- K873124 — ANCHOR BIOPSY NEEDLE
- K831648 — ANCHOR BRAND SURGICAL NEEDLES
- K790405 — ANCHOR BRAND COUNT-TAINER
Data sourced from openFDA. This site is unofficial and independent of the FDA.