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
K893897Substantially Equivalent

Semi-Quantitative Assay for Det. of Igg and Igm

Biostar Medical Products, Inc., Arlington VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893897 is the FDA 510(k) clearance record for SEMI-QUANTITATIVE ASSAY FOR DET. OF IGG AND IGM, a class II device, cleared for Biostar Medical Products, Inc. on under FDA product code LKJ (Antinuclear Antibody, Antigen, Control). FDA records list 5 510(k) clearances for Biostar Medical Products, Inc., from to . As of , FDA records show no recalls naming K893897.

Clearance record

Decision date
Received
(24 days to decision)
Product code
LKJ Antinuclear Antibody, Antigen, Control
Regulation
21 CFR 866.5100
Device class
Class II
Review panel
Immunology
Applicant
Biostar Medical Products, Inc. Suite 1203 Crystal Plz. Bld.1, Arlington VA
Third party review
No

Clearances, product code LKJ

Trailing 12 months

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

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