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510(k) K863721

NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE by Norfolk Medical Products, Inc.

K863721 is an FDA 510(k) premarket notification submitted by Norfolk Medical Products, Inc. for the device "NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE". The FDA issued a decision of Substantially Equivalent on Oct 14, 1986. Norfolk Medical Products, Inc. has 19 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Oct 14, 1986
Date Received
Sep 23, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Norfolk Medical Products, Inc.

  • K192291 — TidalPort-AP Implantable Apheresis Vascular Access Port (Aug 20, 2020)
  • K112713 — NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS (Oct 27, 2011)
  • K102385 — NORFOLK MEDICAL NORPORT FAMILY OF PORTS (Jan 14, 2011)
  • K942784 — NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED (May 2, 1995)
  • K896544 — MD2 PERSONAL INFUSION SYSTEM (May 2, 1990)
  • K872838 — NORFOLK NORPORT (TM) -SP (SKIN PARALLEL) (Aug 25, 1987)
  • K871209 — NORFOLK MEDICAL NORPORT (Jun 24, 1987)
  • K871192 — SUBCUTANEOUSLY IMPLANTED DRUG DELIVERY DEPOT (Jun 10, 1987)
  • K870187 — NORFOLK NORPORT, SUBCUT. IMPLANTED DRUG DEL. DEPOT (May 7, 1987)
  • K870519 — SUBCUTANEOUSLY IMPLANTED DRUG DELIVERY DEPOT (Apr 15, 1987)

FDA data resources