MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT— 510(k) K931197

Name: FDA 510(k) clearance K931197
Creator: U.S. Food and Drug Administration
Published: 1993-09-23

Substantially Equivalent

Meddev International Corp.

FDA 510(k) clearance K931197 for MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT, Substantially Equivalent on 1993-09-23. Applicant: Meddev International Corp.. Device class: 1.

Clearance details

Applicant: Meddev International Corp.
Product code: Code KZF
Device class: Class 1
Regulation: 21 CFR 880.6320
Advisory panel: General Hospital
Date received: 1993-03-09
Decision date: 1993-09-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Altos, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KZF

view all

K954943 — NEVOSCOPE1996-03-27
K952835 — WELCH ALLYN VIDEO EPISCOPE1995-09-22
K945507 — H 5100, H 5200, H 53001994-12-09
K941869 — SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG1994-08-03
K936088 — WAVE FLUORESCENT MAGNIFIER1994-04-26

More clearances from Meddev International Corp.

view all

K940284 — MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION1994-02-28
K874562 — SECURATRODE1988-01-28
K771435 — URINARY LEG BAG, STEOILE1977-09-20

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