510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K981338Substantially Equivalent

Ld-1

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

K981338 is the FDA 510(k) clearance record for LD-1, a class II device, cleared for Abbott Laboratories on under FDA product code JGF (Differential Rate Kinetic Method, Lactate Dehydrogenase Isoenzymes). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K981338.

Clearance record

Decision date
Received
(35 days to decision)
Product code
JGF Differential Rate Kinetic Method, Lactate Dehydrogenase Isoenzymes
Regulation
21 CFR 862.1445
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Abbott Laboratories 1920 Hurd Dr., Irving TX
510(k) summary
Summary
Third party review
No

Clearances, product code JGF

Trailing 12 months

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

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