NEEDLE, PNEUMOPERITONEUM, SPRING LOADED— 510(k) K930474

Name: FDA 510(k) clearance K930474
Creator: U.S. Food and Drug Administration
Published: 1993-07-23

Substantially Equivalent

Ranfac, Corp.

FDA 510(k) clearance K930474 for NEEDLE, PNEUMOPERITONEUM, SPRING LOADED, Substantially Equivalent on 1993-07-23. Applicant: Ranfac, Corp.. Device class: 2.

Clearance details

Applicant: Ranfac, Corp.
Product code: Code FHO
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1993-01-28
Decision date: 1993-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Avon, MA, US

Download summary PDF View on FDA.gov ↗

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