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

KINGS BAY PRELUDE ONE STEP HCG COMBO KIT

K Number: K931698 · Decision Nov 5, 1993
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
1
Review Days
213

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Basic Information

Device Name
KINGS BAY PRELUDE ONE STEP HCG COMBO KIT
K Number
K931698
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
King'S Bay Intl., Inc.
Date Received
April 6, 1993
Decision Date
November 5, 1993
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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