510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K083922Substantially Equivalent

Micrus Microcatheter, Courier Flex, Model Msf 170000-00

Micrus Endovascular Corporation, San Jose CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K083922 is the FDA 510(k) clearance record for MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00, a class II device, cleared for Micrus Endovascular Corporation on under FDA product code DQO (Catheter, Intravascular, Diagnostic). FDA records list 23 510(k) clearances for Micrus Endovascular Corporation, from to . As of , FDA records show no recalls naming K083922.

Clearance record

Decision date
Received
(126 days to decision)
Product code
DQO Catheter, Intravascular, Diagnostic
Regulation
21 CFR 870.1200
Device class
Class II
Review panel
Cardiovascular
Applicant
Micrus Endovascular Corporation 821 Fox Ln., San Jose CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DQO

Trailing 12 months
3 clearances under product code DQO in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DQO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20261
July 20260
August 20260
September 20260
October 20260