Device Listing 1990480108

Listing Summary#

Listing key: 1990480108
Premarket submission: K092300
Device: MODIFICATION TO D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KIT
Applicant: Diagnostic Hybrids, Inc.
Product code: GNW
Decision date: 2009-08-28

Registration key, Registration, FEI table
Registration key	Registration	FEI	Company	Status	Initial importer	Expiration	Address
13086	1528450	1000122536	QUIDEL CORPORATION	1	N	2020-04-25	2005 East State Street, Suite 100 ATHENS OH US 45701