510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K191290Substantially Equivalent

Ancora Nerve Block Catheter Set

Ancora Medical Technology, Menlo Park CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K191290 is the FDA 510(k) clearance record for Ancora Nerve Block Catheter Set, a class II device, cleared for Ancora Medical Technology on under FDA product code BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)). FDA records list one 510(k) clearance for Ancora Medical Technology. As of , FDA records show no recalls naming K191290.

Clearance record

Decision date
Received
(269 days to decision)
Product code
BSP Needle, Conduction, Anesthetic (W/Wo Introducer)
Regulation
21 CFR 868.5150
Device class
Class II
Review panel
Anesthesiology
Applicant
Ancora Medical Technology 333 Ravenswood Ave., Menlo Park CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BSP

Trailing 12 months

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

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