#157 EXAM LIGHT— 510(k) K893949

Substantially Equivalent

Medmark, Inc.

FDA 510(k) clearance K893949 for #157 EXAM LIGHT, Substantially Equivalent on 1989-08-07. Applicant: Medmark, Inc.. Device class: 1.

Clearance details

Applicant: Medmark, Inc.
Product code: Code KFK
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1989-06-01
Decision date: 1989-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Versailles, OH, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KFK

K894301 — MICRO-AIRE STERNUM SAW 48001989-08-03
K870157 — OSCILLATING SAW/ RECIPROCATING SAW/ DRILL-REAMER1987-02-24
K801737 — STERNUM SAW1980-08-20

More clearances from Medmark, Inc.

K914498 — POWDER FREE, NON-STERILE, LATEX EXAMINATION GLOVES1991-11-27
K894987 — MODEL #520/525 ED/RECOVERY STRETCHER1989-09-05

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