510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K122661Substantially Equivalent

Vital 5 Releaf Catheter

Vital 5, North Logan UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K122661 is the FDA 510(k) clearance record for VITAL 5 RELEAF CATHETER, a class II device, cleared for Vital 5 on under FDA product code BSO (Catheter, Conduction, Anesthetic). FDA records list one 510(k) clearance for Vital 5. As of , FDA records show no recalls naming K122661.

Clearance record

Decision date
Received
(180 days to decision)
Product code
BSO Catheter, Conduction, Anesthetic
Regulation
21 CFR 868.5120
Device class
Class II
Review panel
Anesthesiology
Applicant
Vital 5 570 Research Park Way, North Logan UT
510(k) summary
Summary PDF
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