510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K823201Substantially Equivalent

Human Placental Lactogen Kit

Siemens Healthcare Diagnostics Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K823201 is the FDA 510(k) clearance record for HUMAN PLACENTAL LACTOGEN KIT, a class II device, cleared for Diagnostic Products Corp. on under FDA product code JMF (Radioimmunoassay, Human Placental Lactogen). FDA records list 1,204 510(k) clearances for Siemens Healthcare Diagnostics Inc., from to . As of , FDA records show no recalls naming K823201.

Clearance record

Decision date
Received
(34 days to decision)
Product code
JMF Radioimmunoassay, Human Placental Lactogen
Regulation
21 CFR 862.1585
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Diagnostic Products Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JMF

Trailing 12 months

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

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