SURGICAL LIGHT - CHALLENGE 22 SERIES— 510(k) K761018

Substantially Equivalent

Amsco Co.

FDA 510(k) clearance K761018 for SURGICAL LIGHT - CHALLENGE 22 SERIES, Substantially Equivalent on 1977-01-26. Applicant: Amsco Co.. Device class: 2.

Clearance details

Applicant: Amsco Co.
Product code: Code FQP
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1976-11-10
Decision date: 1977-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FQP

K001223 — ACULUX, MODEL AX3001, AX30022000-06-23
K993314 — SYNTHES LIGHT GUIDE1999-12-06
K781581 — SURGICAL LIGHT 22 SERIES1978-10-17
K770812 — HANDLES, LIGHT, SURGICAL, STEOILE1977-05-23

More clearances from Amsco Co.

K912471 — EAGLE 3000 SDS1992-06-26
K854922 — AMSCO POLARIS SL1986-01-24
K833187 — HALL OSTEON1983-10-31
K832945 — EAGLE 2000 STERILIZER SERIES GAS/AERA1983-10-19
K831086 — CEILING MOUNTED SUPPORT1983-08-12

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