FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BIOCIRCUITS IOS QUANTITATIVE HCG TEST CARTRIDGES/BIOCIRCUITS IOS IMMUNOASSAY CONTROLS

K Number: K963770 · Decision Dec 5, 1996
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
8
Review Days
77

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Basic Information

Device Name
BIOCIRCUITS IOS QUANTITATIVE HCG TEST CARTRIDGES/BIOCIRCUITS IOS IMMUNOASSAY CONTROLS
K Number
K963770
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biocircuits Corp.
Date Received
September 19, 1996
Decision Date
December 5, 1996
Product Code
JJY
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
JJY Multi-Analyte Controls, All Kinds (Assayed)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JJY), ordered by most recent decision date.

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Other Clearances by Biocircuits Corp.

K Number Device Name
K981634 BIOCIRCUITS IOS PROSTATE SPECIFIC ANTIGEN (PSA) TEST CARTRIDGES, BIOCIRCUITS IOS PSA CONTROLS
K980819 BIOCIRCUITS IOS FREE THYROXINE (FT4) TEST CARTRIDGES BIOCIRCUITS IOS CONTROLS
K961566 BIOCIRCUITS IOS TSH TEST CARTRIDGES/THYROID CONTROLS
K961792 BIOCIRCUITS IOS SERUM PREGNANCY TEST CARTRIDGES/IMMUNOASSAY CONTROLS
K952719 BIOCIRCUITS IOS (IN-OFFICE SYSTEM)
K952751 BIOCIRCUITS IOS T4/TU TEST CARTRIDGES
K953837 BIOCIRCUITS IOS T4 TEST CARTRIDGE