LIGHTSCOPE SET— 510(k) K894557

Substantially Equivalent

Optik

FDA 510(k) clearance K894557 for LIGHTSCOPE SET, Substantially Equivalent on 1989-08-07. Applicant: Optik. Device class: 1.

Clearance details

Applicant: Optik
Product code: Code HRW
Device class: Class 1
Regulation: 21 CFR 888.1250
Advisory panel: Orthopedic
Date received: 1989-07-20
Decision date: 1989-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Criftib, MD, US

Download summary PDF View on FDA.gov ↗

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More clearances from Optik

K933776 — OPTIK LAPAROSCOPE1994-03-16
K926166 — COAST VIDEO ENDOSCOPIC IMAGING SYSTEM1993-06-01
K896404 — TITAMED ANTWERP SYSTEM1990-04-16
K896589 — MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERP1989-12-27
K894558 — MINI LIGHTSCOPE SET, LIGHTSCOPE JR. SET1989-08-07

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