MODULAR FIBERSCOPE SYSTEM— 510(k) K843683

Name: FDA 510(k) clearance K843683
Creator: U.S. Food and Drug Administration
Published: 1985-01-18

Substantially Equivalent

Reichert Scientific Instruments

FDA 510(k) clearance K843683 for MODULAR FIBERSCOPE SYSTEM, Substantially Equivalent on 1985-01-18. Applicant: Reichert Scientific Instruments. Device class: 2.

Clearance details

Applicant: Reichert Scientific Instruments
Product code: Code GCP
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1984-09-18
Decision date: 1985-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Morris Plains, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GCP

view all

K954614 — EOS BRAND DISPOSABLE PROCTOSCOPE1996-04-10
K896505 — PORGES UNIVERSAL HANDLES1990-01-30
K896008 — MODEL 6500 MERCURY ARC LIGHT SOURCE1989-12-27
K862424 — STEERABLE CATHETER SYSTEM1986-09-22
K860103 — MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVE1986-02-12

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