HELI-TECH RETRIEVAL BASKET— 510(k) K926040

Name: FDA 510(k) clearance K926040
Creator: U.S. Food and Drug Administration
Published: 1992-12-23

Substantially Equivalent

Cape Tech Medical Products

FDA 510(k) clearance K926040 for HELI-TECH RETRIEVAL BASKET, Substantially Equivalent on 1992-12-23. Applicant: Cape Tech Medical Products. Device class: 2.

Clearance details

Applicant: Cape Tech Medical Products
Product code: Code LQR
Device class: Class 2
Regulation: 21 CFR 876.5010
Advisory panel: Gastroenterology, Urology
Date received: 1992-12-01
Decision date: 1992-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Falmouth, MA, US

Download summary PDF View on FDA.gov ↗

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