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

HCG IRMA II

K Number: K891770 · Decision May 24, 1989
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
374
Applicant Total
29
Review Days
61

Basic Information

Device Name
HCG IRMA II
K Number
K891770
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
PACIFIC BIOTECH, INC.
Date Received
March 24, 1989
Decision Date
May 24, 1989
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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K895390 CARDS O.S. (TM) HCG-URINE
K884616 FIRSTDAY EARLY PREGNANCY TESTING KIT II
K883742 MODIFIED TSH IRMA KIT
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K882895 MODIFIED BETA QUIK STAT EIA KIT
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