ULCER WOUND TRAY— 510(k) K922828

Unknown

Ulti-Med Intl., Inc.

FDA 510(k) clearance K922828 for ULCER WOUND TRAY, Unknown on 1992-09-28. Applicant: Ulti-Med Intl., Inc.. Device class: 2.

Clearance details

Applicant: Ulti-Med Intl., Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1992-06-12
Decision date: 1992-09-28
Decision: Unknown
Clearance type: Traditional
Location: Glendale Hts., IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Ulti-Med Intl., Inc.

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K923176 — SURGICAL INSTRUMENT KIT, DISPOSABLE1993-06-17
K920989 — SURGICAL INSTRUMENT KIT, DISPOSABLE1992-10-19
K914244 — STERILE CUSTOM SURGICAL KITS1992-02-24

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