FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

WHOLEPOWER Pregnancy Rapid Test Cassette, WHOLEPOWER Pregnancy Rapid Test Strip, WHOLEPOWER Pregnancy Rapid Test Midstream

K Number: K190705 · Decision Apr 15, 2019
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
225
Applicant Total
1
Review Days
27

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Basic Information

Device Name
WHOLEPOWER Pregnancy Rapid Test Cassette, WHOLEPOWER Pregnancy Rapid Test Strip, WHOLEPOWER Pregnancy Rapid Test Midstream
K Number
K190705
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wholepower Biotech Co., Ltd.
Date Received
March 19, 2019
Decision Date
April 15, 2019
Product Code
LCX
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
LCX Kit, Test, Pregnancy, Hcg, Over The Counter

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