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
K052826Substantially Equivalent

Qms Quinidine. Qms Quinidine Calibrators

Seradyn, Inc., Indianapolis IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K052826 is the FDA 510(k) clearance record for QMS QUINIDINE. QMS QUINIDINE CALIBRATORS, a class II device, cleared for Seradyn, Inc. on under FDA product code LBZ (Enzyme Immunoassay, Quinidine). FDA records list 30 510(k) clearances for Seradyn, Inc., from to . As of , FDA records show no recalls naming K052826.

Clearance record

Decision date
Received
(79 days to decision)
Product code
LBZ Enzyme Immunoassay, Quinidine
Regulation
21 CFR 862.3320
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Seradyn, Inc. 7998 Georgetown Rd., Indianapolis IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LBZ

Trailing 12 months

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

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