RING HANDLE & RETRACTORS— 510(k) K772381

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K772381 for RING HANDLE & RETRACTORS, Substantially Equivalent on 1978-01-17. Applicant: Edward Weck, Inc.. Device class: 1.

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code KAL
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Date received: 1977-12-27
Decision date: 1978-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KAL

K870758 — SMALL MASTOID RETRACTOR1987-03-04
K833604 — ADJUSTABLE FORK RETRACTOR1984-01-03
K772392 — ALLPORT MASTOID RETRACTORS1978-01-17
K760851 — CONVERSE ALTAR RETRACTOR1977-03-10

More clearances from Edward Weck, Inc.

K915378 — WECK TROCAR1992-06-29
K914690 — LM15(TM), CATALOG NUMBER - 5238211992-03-23
K911915 — HEMOCLIP II1992-01-09
K914470 — PNEUMO-SEAL(TM)1991-11-29
K911272 — ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 1147051991-07-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.