510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K934178Substantially Equivalent

Accuscreen 17-Hydroxyprogesterone

Neometrics, Inc., E. Northport NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K934178 is the FDA 510(k) clearance record for ACCUSCREEN 17-HYDROXYPROGESTERONE, a class I device, cleared for Neometrics, Inc. on under FDA product code JLX (Radioimmunoassay, 17-Hydroxyprogesterone). FDA records list 21 510(k) clearances for Neometrics, Inc., from to . As of , FDA records show no recalls naming K934178.

Clearance record

Decision date
Received
(580 days to decision)
Product code
JLX Radioimmunoassay, 17-Hydroxyprogesterone
Regulation
21 CFR 862.1395
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Neometrics, Inc. 104bellerose Ave., E. Northport NY
510(k) summary
Statement
Third party review
No

Clearances, product code JLX

Trailing 12 months

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

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