Cleared Traditional

K791978 - SUGITA ANEURYSM CLIPS, APPLIERS & CASE (FDA 510(k) Clearance)

K791978 · Codman & Shurtleff, Inc. · Neurology device
Sep 1979
Decision
-
Days
-
Risk

K791978 is an FDA 510(k) clearance for the SUGITA ANEURYSM CLIPS, APPLIERS & CASE..

Submitted by Codman & Shurtleff, Inc. (Mchenry, US). The FDA issued a Cleared decision on September 28, 1979.

This device falls under the Neurology FDA review panel.

Submission Details

510(k) Number K791978 FDA.gov
FDA Decision Cleared Substantially Equivalent - Product Development Protocol (SESP)
Date Received September 28, 1979
Decision Date September 28, 1979
Days to Decision -
Submission Type Traditional
Review Panel Neurology (NE)
Summary -

Device Classification

Product Code -
Device Class -