510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K860924Substantially Equivalent

Ramp Progesturine Pdg Assay--48 Test Kit

Monoclonal Antibodies, Inc., Mountain View CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860924 is the FDA 510(k) clearance record for RAMP PROGESTURINE PDG ASSAY--48 TEST KIT, a class I device, cleared for Monoclonal Antibodies, Inc. on under FDA product code JLS (Radioimmunoassay, Progesterone). FDA records list 14 510(k) clearances for Monoclonal Antibodies, Inc., from to . As of , FDA records show no recalls naming K860924.

Clearance record

Decision date
Received
(113 days to decision)
Product code
JLS Radioimmunoassay, Progesterone
Regulation
21 CFR 862.1620
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Monoclonal Antibodies, Inc. 2319 Charleston Rd., Mountain View CA
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