NEEDLEHOLDER, MICROVASULAR 5 1/2— 510(k) K780154

Name: FDA 510(k) clearance K780154
Creator: U.S. Food and Drug Administration
Published: 1978-03-17

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K780154 for NEEDLEHOLDER, MICROVASULAR 5 1/2, Substantially Equivalent on 1978-03-17. Applicant: Edward Weck, Inc.. Device class: 1.

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code HNM
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1978-01-30
Decision date: 1978-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HNM

view all

K844448 — OMS/GONVERS RETINAL PERFORATOR1985-08-21

More clearances from Edward Weck, Inc.

view all

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.