FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CONTRAST STRIP HCG

K Number: K964156 · Decision Nov 25, 1996
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
5
Review Days
40

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Basic Information

Device Name
CONTRAST STRIP HCG
K Number
K964156
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genzyme Diagnostics
Date Received
October 16, 1996
Decision Date
November 25, 1996
Product Code
JHI
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JHI Visual, Pregnancy Hcg, Prescription Use

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JHI), ordered by most recent decision date.

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Other Clearances by Genzyme Diagnostics

K Number Device Name
K043385 OSOM HCG COMBO TEST
K983399 GIARDIA/CRYPTOSPORIDIUM COMBO RAPID ASSAY
K963425 GENZYME DIAGNOSTICS CONTRAST MONO
K964155 CONTRAST HCG URINE/SERUM TEST AND RAPID HCG URINE/SERUM TEST