510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925018Unknown

IV Prep Kit W/o Dressing (Non-Sterile)

Customed, Inc, Fajardo PR / Traditional, Unknown
FDA source (opens on fda.gov)

K925018 is the FDA 510(k) clearance record for IV PREP KIT W/O DRESSING (NON-STERILE), a class II device, cleared for Customed, 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 37 510(k) clearances for Customed, Inc., from to . As of , FDA records show no recalls naming K925018.

Clearance record

Decision date
Received
(337 days to decision)
Product code
LRS I.V. Start Kit
Regulation
21 CFR 880.5200
Device class
Class II
Review panel
General Hospital
Applicant
Customed, Inc. Calle Igualdad #7, Fajardo PR
510(k) summary
Statement
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