510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K900710Substantially Equivalent

Interflo Medical Model F-1 Thermodilution Catheter

Intec Medical, Inc., Plano TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900710 is the FDA 510(k) clearance record for INTERFLO MEDICAL MODEL F-1 THERMODILUTION CATHETER, a class II device, cleared for Intec Medical, Inc. on under FDA product code KRB (Probe, Thermodilution). FDA records list 17 510(k) clearances for Intec Medical, Inc., from to . As of , FDA records show no recalls naming K900710.

Clearance record

Decision date
Received
(247 days to decision)
Product code
KRB Probe, Thermodilution
Regulation
21 CFR 870.1915
Device class
Class II
Review panel
Cardiovascular
Applicant
Intec Medical, Inc. 1101 Resource Dr., Plano TX
Third party review
No

Clearances, product code KRB

Trailing 12 months

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

FDA records show no clearances under product code KRB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KRB, 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