ALLIGATOR CUP FORCEPS— 510(k) K772396

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K772396 for ALLIGATOR CUP FORCEPS, Substantially Equivalent on 1978-01-17. Applicant: Edward Weck, Inc.. Device class: 1.

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code KAE
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

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Recent devices under product code KAE

K853708 — LARYNGASCOPES, FORCEPS, MICRO SUCTION TUBE & REFLE1986-02-14
K851775 — 19-790 TO 19-1042 DRESSING/SPONGE FORCEPS1985-06-11
K851794 — 41-180 TO 41-246 VARIOUS NASAL FORCEPS1985-06-11
K851795 — 41-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPS1985-06-11
K833608 — GOLD ALLIGATOR FORCEPS1984-01-11

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.