510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K964301Substantially Equivalent

N-Assay Tia Multi V-Nl

Crestat Diagnostics, Inc., Murrieta CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K964301 is the FDA 510(k) clearance record for N-ASSAY TIA MULTI V-NL, a class II device, cleared for Crestat Diagnostics, Inc. on under FDA product code DAD (Haptoglobin, Antigen, Antiserum, Control). FDA records list 29 510(k) clearances for Crestat Diagnostics, Inc., from to . As of , FDA records show no recalls naming K964301.

Clearance record

Decision date
Received
(258 days to decision)
Product code
DAD Haptoglobin, Antigen, Antiserum, Control
Regulation
21 CFR 866.5460
Device class
Class II
Review panel
Immunology
Applicant
Crestat Diagnostics, Inc. 25549 Adams Ave., Murrieta CA
510(k) summary
Statement
Third party review
No

Clearances, product code DAD

Trailing 12 months

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

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