GESCO CATHETERIZATION TRAY— 510(k) K882647

Unknown

Gesco Intl., Inc.

FDA 510(k) clearance K882647 for GESCO CATHETERIZATION TRAY, Unknown on 1988-09-09. Applicant: Gesco Intl., Inc.. Device class: 1.

Clearance details

Applicant: Gesco Intl., Inc.
Product code: Code GBQ
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1988-06-27
Decision date: 1988-09-09
Decision: Unknown
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

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