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

ACON HCG ONE STEP PREGNANCY TEST DEVICE (URINE)

K Number: K993317 · Decision Dec 1, 1999
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
374
Applicant Total
68
Review Days
58

Basic Information

Device Name
ACON HCG ONE STEP PREGNANCY TEST DEVICE (URINE)
K Number
K993317
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ACON LABORATORIES, INC.
Date Received
October 4, 1999
Decision Date
December 1, 1999
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

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