510(k) K882086

Device
Qtest(tm) Pregnancy
Applicant
QUIDEL CORP.
510(k) number
K882086
Product code
JHI
Decision
Substantially Equivalent (SESE)
Decision date
1988-07-28
Date received
1988-05-18
Regulation
862.1155
Classification name
Visual, Pregnancy Hcg, Prescription Use
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
Robin Weiner
Address
11077 N. Torrey Pines Rd. La Jolla CA US 92037 92037

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code JHI#

510(k), Device, Applicant table
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K112101FASTEP HCG PREGANCY SERUM/URINE CASSETTE AND DIPSTICK TESTSPolymed Therapeutics, Inc.2012-07-17
K112315HOME PREGNANCY TESTNewscen Coast Bio-Pharmaceutical Co., Ltd.2012-04-23
K102175RAPIDVUE HCG TESTQuidel Corporation2010-08-25
K072264FASTPACK HCG IMMUNOASSAYQualigen, Inc.2007-12-06
K070921BIONEXIA HCG PREGNANCY CASSETTE AND DIPSTICK TESTS, MODEL 08-HCG AND 02-HCGApplied Dna Technologies, Inc.2007-06-29