Cleared Traditional

K863721 - NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE (FDA 510(k) Clearance)

K863721 · Norfolk Medical Products, Inc. · General & Plastic Surgery device
Oct 1986
Decision
21d
Days
-
Risk

K863721 is an FDA 510(k) clearance for the NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE..

Submitted by Norfolk Medical Products, Inc. (Skokie, US). The FDA issued a Cleared decision on October 14, 1986, 21 days after receiving the submission on September 23, 1986.

This device falls under the General & Plastic Surgery FDA review panel.

Submission Details

510(k) Number K863721 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 23, 1986
Decision Date October 14, 1986
Days to Decision 21 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -

Device Classification

Product Code -
Device Class -