DOUBLETIME 2-TIPPED APPLIERS FOR HEMOCLI— 510(k) K800318

Name: FDA 510(k) clearance K800318
Creator: U.S. Food and Drug Administration
Published: 1980-03-10

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K800318 for DOUBLETIME 2-TIPPED APPLIERS FOR HEMOCLI, Substantially Equivalent on 1980-03-10. Applicant: Edward Weck, Inc.. Device class: 1.

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code HBT
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1980-02-12
Decision date: 1980-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code HBT

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K924929 — REFLEX(R) ECA1993-07-21
K896262 — TITANIUM LIGATING CLIPS1990-01-02
K862696 — TEMPORARY HEMO CLIP, 07-096-01/02 & APPLY FORCEP1986-07-30

More clearances from Edward Weck, Inc.

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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

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