510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K070206Substantially Equivalent

Diagnostic Hybrids D3 Dfa Varicella-Zoster Virus Identification Kit, 01-020000

Ortho-Clinical Diagnostics, Inc., Athens OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K070206 is the FDA 510(k) clearance record for DIAGNOSTIC HYBRIDS D3 DFA VARICELLA-ZOSTER VIRUS IDENTIFICATION KIT, 01-020000, a class II device, cleared for Diagnostic Hybrids, Inc. on under FDA product code GQW (Antigen, Cf, (Including Cf Control), Varicella-Zoster). FDA records list 311 510(k) clearances for ORTHO-CLINICAL DIAGNOSTICS, INC., from to . As of , FDA records show no recalls naming K070206.

Clearance record

Decision date
Received
(220 days to decision)
Product code
GQW Antigen, Cf, (Including Cf Control), Varicella-Zoster
Regulation
21 CFR 866.3900
Device class
Class II
Review panel
Microbiology
Applicant
Diagnostic Hybrids, Inc. 350 W. State St., Athens OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GQW

Trailing 12 months

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

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