510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K801552Substantially Equivalent

Mod. 9542 Flow-Thru Inject. Temp. Sensor

Edwards Laboratories, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K801552 is the FDA 510(k) clearance record for MOD. 9542 FLOW-THRU INJECT. TEMP. SENSOR, a class II device, cleared for Edwards Laboratories on under FDA product code KRB (Probe, Thermodilution). FDA records list 12 510(k) clearances for Edwards Laboratories, from to . As of , FDA records show no recalls naming K801552.

Clearance record

Decision date
Received
(20 days to decision)
Product code
KRB Probe, Thermodilution
Regulation
21 CFR 870.1915
Device class
Class II
Review panel
Cardiovascular
Applicant
Edwards Laboratories 803 N. Front St. Suite 3, Mchenry IL
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