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
K980059Substantially Equivalent

Seraquest Mumps Igg

Quest Intl., Inc., North Miami FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980059 is the FDA 510(k) clearance record for SERAQUEST MUMPS IGG, a class I device, cleared for Quest Intl., Inc. on under FDA product code LJY (Enzyme Linked Immunoabsorbent Assay, Mumps Virus). FDA records list 25 510(k) clearances for Quest Intl., Inc., from to . As of , FDA records show no recalls naming K980059.

Clearance record

Decision date
Received
(106 days to decision)
Product code
LJY Enzyme Linked Immunoabsorbent Assay, Mumps Virus
Regulation
21 CFR 866.3380
Device class
Class I
Review panel
Microbiology
Applicant
Quest Intl., Inc. 1938 NE 148th Terr., North Miami FL
510(k) summary
Statement
Third party review
No

Clearances, product code LJY

Trailing 12 months

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

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