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

VISUAL HCG PREGNANCY TEST

K Number: K923376 · Decision Oct 1, 1992
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
36
Review Days
84

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Basic Information

Device Name
VISUAL HCG PREGNANCY TEST
K Number
K923376
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tech-Co, Inc.
Date Received
July 9, 1992
Decision Date
October 1, 1992
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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Other Clearances by Tech-Co, Inc.

K Number Device Name
K921968 IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST
K920766 T4 EIA BEAD ASSAY
K920716 DIRECT PREGNANCY TEST
K902574 POTASSIUM REAGENT SET
K901561 IRON/TOTAL IRON BINDING CAPACITY
K883387 ALANINE AMINO TRANSFERASE (COLORIMETRIC METHOD)
K883683 HEMOGLOBIN
K883386 CHLORIDE
K881172 BILIRUBIN (DIRECT)
K881173 ASPARTATE AMINOTRANSFERASE (COLORIMETRIC METHOD)
Search all 36 clearances from Tech-Co, Inc. →