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

AMERLITE HCG-60 ASSAY, LAN.0083/2083 240KIT/144KIT

K Number: K881355 · Decision Jun 8, 1988
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
374
Applicant Total
94
Review Days
51

Basic Information

Device Name
AMERLITE HCG-60 ASSAY, LAN.0083/2083 240KIT/144KIT
K Number
K881355
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
AMERSHAM CORP.
Date Received
April 18, 1988
Decision Date
June 8, 1988
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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