ULTRASAFE— 510(k) K920059

Substantially Equivalent

Ultrawin Sdn Bhd

FDA 510(k) clearance K920059 for ULTRASAFE, Substantially Equivalent on 1992-03-11. Applicant: Ultrawin Sdn Bhd. Device class: 1.

Clearance details

Applicant
Ultrawin Sdn Bhd
Product code
Code LYY
Device class
Class 1
Regulation
21 CFR 880.6250
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Malaysia, MY
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