MAXIMA FILTERED HARDSHELL RESERVIOR— 510(k) K933496

Name: FDA 510(k) clearance K933496
Creator: U.S. Food and Drug Administration
Published: 1993-10-15

Substantially Equivalent

Medtronic Vascular

FDA 510(k) clearance K933496 for MAXIMA FILTERED HARDSHELL RESERVIOR, Substantially Equivalent on 1993-10-15. Applicant: Medtronic Vascular. Device class: 2.

Clearance details

Applicant: Medtronic Vascular
Product code: Code DTP
Device class: Class 2
Regulation: 21 CFR 870.4230
Advisory panel: Cardiovascular
Date received: 1993-07-19
Decision date: 1993-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

Download summary PDF View on FDA.gov ↗

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