510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K863099Substantially Equivalent

Abbott Testpack (Tm) Acute Hep a Control Kit

Abbott Medical, Abbott Park IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K863099 is the FDA 510(k) clearance record for ABBOTT TESTPACK (TM) ACUTE HEP A CONTROL KIT, a class I device, cleared for Abbott Laboratories on under FDA product code JJK (Oncometer, Plasma, For Clinical Use). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K863099.

Clearance record

Decision date
Received
(34 days to decision)
Product code
JJK Oncometer, Plasma, For Clinical Use
Regulation
21 CFR 862.2720
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Abbott Laboratories One Abbott Park Rd., Abbott Park IL
Third party review
No

Clearances, product code JJK

Trailing 12 months

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

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