510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K001717Substantially Equivalent

Micor Conduction Catheter

Micor, Inc., Allison Park PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K001717 is the FDA 510(k) clearance record for MICOR CONDUCTION CATHETER, a class II device, cleared for Micor, Inc. on under FDA product code BSO (Catheter, Conduction, Anesthetic). FDA records list 5 510(k) clearances for Micor, Inc., from to . As of , FDA records show no recalls naming K001717.

Clearance record

Decision date
Received
(107 days to decision)
Product code
BSO Catheter, Conduction, Anesthetic
Regulation
21 CFR 868.5120
Device class
Class II
Review panel
Anesthesiology
Applicant
Micor, Inc. 2855 Oxford Blvd., Allison Park PA
510(k) summary
Summary
Third party review
No

Clearances, product code BSO

Trailing 12 months

FDA records hold no clearances under product code BSO in the trailing twelve months.

FDA records show no clearances under product code BSO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BSO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260