510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K782009Substantially Equivalent

Ria Kit, Progesterone

The Upjohn Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K782009 is the FDA 510(k) clearance record for RIA KIT, PROGESTERONE, a class I device, cleared for The Upjohn Co. on under FDA product code JLS (Radioimmunoassay, Progesterone). FDA records list 6 510(k) clearances for The Upjohn Co., from to . As of , FDA records show no recalls naming K782009.

Clearance record

Decision date
Received
(91 days to decision)
Product code
JLS Radioimmunoassay, Progesterone
Regulation
21 CFR 862.1620
Device class
Class I
Review panel
Clinical Chemistry
Applicant
The Upjohn Co. 803 N. Front St. Suite 3, Mchenry IL
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