510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K810625Substantially Equivalent

Human Placental Lactogen Radioimmuno-

Serono Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K810625 is the FDA 510(k) clearance record for HUMAN PLACENTAL LACTOGEN RADIOIMMUNO-, a class I device, cleared for Serono Laboratories, Inc. on under FDA product code DHI (Ng3m(Bo), Antigen, Antiserum, Control). FDA records list 10 510(k) clearances for Serono Laboratories, Inc., from to . As of , FDA records show no recalls naming K810625.

Clearance record

Decision date
Received
(18 days to decision)
Product code
DHI Ng3m(Bo), Antigen, Antiserum, Control
Regulation
21 CFR 866.5065
Device class
Class I
Review panel
Immunology
Applicant
Serono Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DHI

Trailing 12 months

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

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