510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K040923Substantially Equivalent

Luminescent Immunoassay Kit for the Detection of Progesterone in Saliva

Ibl GmbH, East Stroudsburg PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K040923 is the FDA 510(k) clearance record for LUMINESCENT IMMUNOASSAY KIT FOR THE DETECTION OF PROGESTERONE IN SALIVA, a class I device, cleared for Ibl GmbH on under FDA product code JLS (Radioimmunoassay, Progesterone). FDA records list 6 510(k) clearances for Ibl GmbH, from to . As of , FDA records show no recalls naming K040923.

Clearance record

Decision date
Received
(105 days to decision)
Product code
JLS Radioimmunoassay, Progesterone
Regulation
21 CFR 862.1620
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Ibl GmbH 150 Cherry Ln. Rd., East Stroudsburg PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JLS

Trailing 12 months

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

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