510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K170112Substantially Equivalent

IMD's Lumbar Puncture Needle

International Medical Development, Inc.(Imd), Huntsville UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K170112 is the FDA 510(k) clearance record for IMD's Lumbar Puncture Needle, a class II device, cleared for International Medical Development, Inc.(Imd) on under FDA product code BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)). FDA records list one 510(k) clearance for International Medical Development, Inc.(Imd). As of , FDA records show no recalls naming K170112.

Clearance record

Decision date
Received
(386 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
International Medical Development, Inc.(Imd) 560 Hwy. 39 (P.O. Box 510), Huntsville UT
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