510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K991886Substantially Equivalent

Pulsion Pulsiocath, Pulsion Pcco Monitoring Kit, Pulsion in-Line Injectate Sensor

Pulsion Medical Systems AG, Wilmington NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K991886 is the FDA 510(k) clearance record for PULSION PULSIOCATH, PULSION PCCO MONITORING KIT, PULSION IN-LINE INJECTATE SENSOR, a class II device, cleared for Pulsion Medical Systems, Inc. on under FDA product code KRB (Probe, Thermodilution). FDA records list 8 510(k) clearances for Pulsion Medical Systems, Inc., from to . As of , FDA records show one recall naming K991886.

Clearance record

Decision date
Received
(344 days to decision)
Product code
KRB Probe, Thermodilution
Regulation
21 CFR 870.1915
Device class
Class II
Review panel
Cardiovascular
Applicant
Pulsion Medical Systems, Inc. 8911 Sedgley Dr., Wilmington NC
510(k) summary
Summary
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