510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K871281Substantially Equivalent

IV Start Kit

The Jarid Group, Inc., Wayside NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K871281 is the FDA 510(k) clearance record for IV START KIT, a class II device, cleared for The Jarid Group, Inc. on under FDA product code LRS (I.V. Start Kit). FDA's definition for product code LRS reads: "This product code has been established in accordance with the May 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at...". FDA records list 3 510(k) clearances for The Jarid Group, Inc., from to . As of , FDA records show no recalls naming K871281.

Clearance record

Decision date
Received
(57 days to decision)
Product code
LRS I.V. Start Kit
Regulation
21 CFR 880.5200
Device class
Class II
Review panel
General Hospital
Applicant
The Jarid Group, Inc. 41 Ascot Dr., Wayside NJ
Third party review
No

Clearances, product code LRS

Trailing 12 months

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

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