510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932800Substantially Equivalent

Cardima Tracker(r) Infusion Catheter

Cardima, Inc., Fremont CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932800 is the FDA 510(k) clearance record for CARDIMA TRACKER(R) INFUSION CATHETER, a class II device, cleared for Cardima, Inc. on under FDA product code KRA (Catheter, Continuous Flush). FDA records list 12 510(k) clearances for Cardima, Inc., from to . As of , FDA records show no recalls naming K932800.

Clearance record

Decision date
Received
(195 days to decision)
Product code
KRA Catheter, Continuous Flush
Regulation
21 CFR 870.1210
Device class
Class II
Review panel
Cardiovascular
Applicant
Cardima, Inc. 47201 Lakeview Blvd., Fremont CA
510(k) summary
Summary
Third party review
No

Clearances, product code KRA

Trailing 12 months
5 clearances under product code KRA in the twelve months to October 2026, September 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KRA, 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 20262
October 20260