SURGICAL INSTRUMENT KIT, DISPOSABLE— 510(k) K923176

Substantially Equivalent

Ulti-Med Intl., Inc.

FDA 510(k) clearance K923176 for SURGICAL INSTRUMENT KIT, DISPOSABLE, Substantially Equivalent on 1993-06-17. Applicant: Ulti-Med Intl., Inc.. Device class: 1.

Clearance details

Applicant
Ulti-Med Intl., Inc.
Product code
Code KDD
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Glendale Hts., IL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code KDD

view all

More clearances from Ulti-Med Intl., Inc.

view all

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