NEEDLES, DESIGN CHANGE, IV CATHETERS— 510(k) K780896

Name: FDA 510(k) clearance K780896
Creator: U.S. Food and Drug Administration
Published: 1978-08-23

Substantially Equivalent

Jelco Laboratories

FDA 510(k) clearance K780896 for NEEDLES, DESIGN CHANGE, IV CATHETERS, Substantially Equivalent on 1978-08-23. Applicant: Jelco Laboratories. Device class: 1.

Clearance details

Applicant: Jelco Laboratories
Product code: Code GCB
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1978-05-30
Decision date: 1978-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: KS, US

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