510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K874258Substantially Equivalent

Ventrescreen, Hcg Urine

Ventrex Laboratories, Inc., Portland ME / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K874258 is the FDA 510(k) clearance record for VENTRESCREEN, HCG URINE, a class II device, cleared for Ventrex Laboratories, Inc. on under FDA product code JHI (Visual, Pregnancy Hcg, Prescription Use). FDA records list 82 510(k) clearances for Ventrex Laboratories, Inc., from to . As of , FDA records show no recalls naming K874258.

Clearance record

Decision date
Received
(34 days to decision)
Product code
JHI Visual, Pregnancy Hcg, Prescription Use
Regulation
21 CFR 862.1155
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Ventrex Laboratories, Inc. 217 Read St., Portland ME
Third party review
No

Clearances, product code JHI

Trailing 12 months
1 clearance under product code JHI in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JHI, 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 20261
October 20260