ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTER— 510(k) K900160

Name: FDA 510(k) clearance K900160
Creator: U.S. Food and Drug Administration
Published: 1990-01-24

Substantially Equivalent

Jedmed Instrument Co.

FDA 510(k) clearance K900160 for ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTER, Substantially Equivalent on 1990-01-24. Applicant: Jedmed Instrument Co.. Device class: 1.

Clearance details

Applicant: Jedmed Instrument Co.
Product code: Code KQM
Device class: Class 1
Regulation: 21 CFR 878.4160
Advisory panel: General, Plastic Surgery
Date received: 1990-01-12
Decision date: 1990-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQM

view all

K890826 — SONY VIDEO GRAPHIC PRINTER UP-8501989-03-14
K885042 — SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD1988-12-22
K882958 — SONY VIDEO PRINTERS, UP SERIES1988-08-04
K882924 — MEDICAM MC-7 AND RP-7 SURGICAL CAMERAS1988-07-26
K873419 — VIDEO PRINTER SYSTEM1987-11-02

More clearances from Jedmed Instrument Co.

view all

K132039 — ERGO-FLEX LARYNGO-NASOPHARYNGOSCOPE EF-N AND EF-N SLIM2014-02-21
K021750 — LID CHAIN EYELID WEIGHTS2003-01-27
K954184 — JED-LIGHT FIBEROPTIC LIGHT SOURCE1995-11-13
K944032 — VIDEO SCOPE SYSTEM (LARYNGOSCOPE)1995-09-15
K950925 — JEDMED LARYNGEAL SCOPE1995-08-11

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