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510(k) K790405

ANCHOR BRAND COUNT-TAINER by Anchor Products Co. — Product Code MMK

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 26, 1979
Date Received
February 26, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Container, Sharps
Device Class
Class II
Regulation Number
880.5570
Review Panel
HO
Submission Type

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  • K873124 — ANCHOR BIOPSY NEEDLE (September 8, 1987)
  • K831648 — ANCHOR BRAND SURGICAL NEEDLES (August 16, 1983)

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