510(k) Report

510(k) · Cleared

Cleared

Norfolk Medical Posi-Grip 'Huber Point' Needle

K863721510(k) TraditionalCleared Oct 14, 198621-day review

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Norfolk Medical Products, Inc.

Cleared on Oct 14, 1986 after a 21-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Oct 14, 1986
Review
21 days
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2015: 1 descendant cleared1990200020102020
  1. This deviceK863721 Norfolk Medical Posi-Grip 'Huber Point' NeedleNorfolk Medical Products, Inc. · 1986
  2. Descendant · cites it directly · 0 of its ownK151341 Turbo High-Flow Non-coring NeedleNorfolk Medical · 2015

Most influential descendants

Showing 1 of 1 · See all
  • K151341Turbo High-Flow Non-coring NeedleNorfolk Medical · 2015 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K863721Norfolk Medical Posi-Grip 'Huber Point' NeedleNorfolk Medical Products, Inc.1986—
+1K151341Turbo High-Flow Non-coring NeedleNorfolk Medical2015—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
FIG. 1 — Lineage of K863721, 1986–2015Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K151341Turbo High-Flow Non-coring NeedleNorfolk Medical20150

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K151341 (Norfolk Medical, 2015) has gone furthest, with 0 descendants of its own.

More from Norfolk Medical Products, Inc.

20 FDA decisions under this applicant name. See the company

  • K192291TidalPort-AP Implantable Apheresis Vascular Access PortNorfolk Medical Products, Inc. · 2020
  • K112713Norfolk Medical-Sportport-Family of PortsNorfolk Medical Products, Inc. · 2011
  • K102385Norfolk Medical Norport Family of PortsNorfolk Medical Products, Inc. · 2011
  • K942784Norfolk Omega Port-LP Subcutaneously ImplantedNorfolk Medical Products, Inc. · 1995
  • K896544MD2 Personal Infusion SystemNorfolk Medical Products, Inc. · 1990

https://510kreport.com/device/K863721 · printed Nov 6, 2026

Cite this page

510(k) Report. “K863721: Norfolk Medical Posi-Grip 'Huber Point' Needle.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K863721

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026