Atlas FDA

BIONEXIA HCG PREGNANCY CASSETTE AND DIPSTICK TESTS, MODEL 08-HCG AND 02-HCG

FDA 510(k) clearance K070921 · decided 2007-06-29

Clearance details

K-number
K070921
Device name
BIONEXIA HCG PREGNANCY CASSETTE AND DIPSTICK TESTS, MODEL 08-HCG AND 02-HCG
Applicant
Applied Dna Technologies, Inc.
Decision
Substantially Equivalent
Date received
2007-04-02
Decision date
2007-06-29
Days to decision
88 days
Clearance type
Traditional
Product code
JHI
Device class
2
Regulation number
862.1155
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Mission Viejo, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
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Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy Serum/Urine Combo Test Strip (K152768)Assure Tech. Co., Ltd.2016-02-24
WUNDER PREGNANCY TEST (K130456)James Nguyen2014-04-08
FASTEP S10 HCG SERUM/URINE COMBO TEST (K132834)Polymed Therapeutics, Inc.2014-01-09
SOFIA(R) HCG FIA (K131166)Quidel Corp.2013-08-02
CHEMTRUE HCG PREGNANCY URINE DIPSTICK, HCG PREGNANCY URINE CASSETTE TEST, AND HCG COMBO SERUM/URINE CASSETTE TEST (K123844)Chemtron Biotech, Inc.2013-05-30
FASTEP HCG PREGANCY SERUM/URINE CASSETTE AND DIPSTICK TESTS (K112101)Polymed Therapeutics, Inc.2012-07-17
HOME PREGNANCY TEST (K112315)Newscen Coast Bio-Pharmaceutical Co., Ltd.2012-04-23
RAPIDVUE HCG TEST (K102175)Quidel Corporation2010-08-25

Recalls involving this device

No recalls on record reference this clearance.