510(k) K914303

Device
Target(tm)-hog
Applicant
V-TECH, INC.
510(k) number
K914303
Product code
JHI
Decision
Substantially Equivalent (SESE)
Decision date
1991-10-11
Date received
1991-09-25
Regulation
862.1155
Classification name
Visual, Pregnancy Hcg, Prescription Use
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
WILLA K BRUNKHORST
Address
270 E. Bonita Ave. Pomona CA US 91767 91767

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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K112315HOME PREGNANCY TESTNewscen Coast Bio-Pharmaceutical Co., Ltd.2012-04-23
K102175RAPIDVUE HCG TESTQuidel Corporation2010-08-25
K072264FASTPACK HCG IMMUNOASSAYQualigen, Inc.2007-12-06
K071030BIONEXIA HCG PREGNANCY SERUM/URINE CASSETTE AND DIPSTICK TESTS, MODELS 08-HCGC AND 02-HCGCApplied Dna Technologies, Inc.2007-06-29
K070921BIONEXIA HCG PREGNANCY CASSETTE AND DIPSTICK TESTS, MODEL 08-HCG AND 02-HCGApplied Dna Technologies, Inc.2007-06-29