LACERATION TRAY— 510(k) K873439

Substantially Equivalent

Ulti-Med Intl., Inc.

FDA 510(k) clearance K873439 for LACERATION TRAY, Substantially Equivalent on 1987-09-11. Applicant: Ulti-Med Intl., Inc.. Device class: 1.

Clearance details

Applicant: Ulti-Med Intl., Inc.
Product code: Code LRP
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-08-27
Decision date: 1987-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Schaumburg, IL, US

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