KCK INDUSTRIES' SURGICAL INSTRUMENTS— 510(k) K871894

Name: FDA 510(k) clearance K871894
Creator: U.S. Food and Drug Administration
Published: 1987-06-23

Substantially Equivalent

Kck Industries

FDA 510(k) clearance K871894 for KCK INDUSTRIES' SURGICAL INSTRUMENTS, Substantially Equivalent on 1987-06-23. Applicant: Kck Industries. Device class: 1.

Clearance details

Applicant: Kck Industries
Product code: Code GDX
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-05-01
Decision date: 1987-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodland Hills, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GDX

view all

K923689 — SURGISTAR BLADES1992-09-09
K921167 — ULTRABLADE1992-07-30
K914086 — ICAN CYLINDRICAL SPONGES1991-10-09
K904505 — CCI CORNEAL SCARIFIER1991-04-23
K905380 — 1-CUT ACL GRAFT KNIFE1990-12-13

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