510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K070317Substantially Equivalent

Zeus Scientific, Inc Vzv Igm Elisa Test System

Zeus Scientific LLC, Branchburg NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K070317 is the FDA 510(k) clearance record for ZEUS SCIENTIFIC, INC VZV IGM ELISA TEST SYSTEM, a class II device, cleared for Zeus Scientific, Inc. on under FDA product code LFY (Enzyme Linked Immunoabsorbent Assay, Varicella-Zoster). FDA records list 141 510(k) clearances for Zeus Scientific, Inc., from to . As of , FDA records show no recalls naming K070317.

Clearance record

Decision date
Received
(153 days to decision)
Product code
LFY Enzyme Linked Immunoabsorbent Assay, Varicella-Zoster
Regulation
21 CFR 866.3900
Device class
Class II
Review panel
Microbiology
Applicant
Zeus Scientific, Inc. 200 Evans Way, Branchburg NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LFY

Trailing 12 months

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

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