510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K802308Substantially Equivalent

T/k (Ata/ama) Universal Biopak

Bioware Products, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802308 is the FDA 510(k) clearance record for T/K (ATA/AMA) UNIVERSAL BIOPAK, a class II device, cleared for Bioware Products on under FDA product code DBM (Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control). FDA records list 4 510(k) clearances for Bioware Products, from to . As of , FDA records show no recalls naming K802308.

Clearance record

Decision date
Received
(69 days to decision)
Product code
DBM Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control
Regulation
21 CFR 866.5090
Device class
Class II
Review panel
Immunology
Applicant
Bioware Products 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code DBM

Trailing 12 months

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

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