LIGHT-PAK— 510(k) K791733

Substantially Equivalent

Midwest

FDA 510(k) clearance K791733 for LIGHT-PAK, Substantially Equivalent on 1979-10-23. Applicant: Midwest. Device class: 1.

Clearance details

Applicant: Midwest
Product code: Code EAY
Device class: Class 1
Regulation: 21 CFR 872.4620
Advisory panel: Dental
Date received: 1979-08-28
Decision date: 1979-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EAY

K953191 — MODEL A15-1011995-09-05
K953192 — MODEL A15-1031995-09-05
K935718 — JEDENTAL VLC DENTAL CURING LIGHT1994-01-26
K871816 — STRYKERSCOPE TM/ORTHOSCOPE TM/STRYKER MINISCOPE TM1987-08-03
K831976 — POWER OPTIC1983-08-12

More clearances from Midwest

K863677 — TRADITION HIGH SPEED HANDPIECE1986-10-06
K850344 — AM-40 POWER OPTIC AIR MOTOR POWER OPTIC CONTRA ANG1985-03-25
K792445 — MW STRAIGHT ATTACHMENT1979-12-06
K792302 — LS-1001979-11-27
K792303 — MW 8000-I1979-11-27

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