Cleared Traditional

K834143 - NYLON COMPRESSION STUMP SHEATH
(FDA 510(k) Clearance)

Jan 1984
Decision
39d
Days
Risk

K834143 is an FDA 510(k) clearance for the NYLON COMPRESSION STUMP SHEATH..

Submitted by Ipos Luneburg (Mchenry, US). The FDA issued a Cleared decision on January 9, 1984, 39 days after receiving the submission on December 1, 1983.

This device falls under the Physical Medicine FDA review panel.

Submission Details

510(k) Number K834143 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 01, 1983
Decision Date January 09, 1984
Days to Decision 39 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary

Device Classification

Product Code
Device Class