FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

MODEL 115-16 PHOSPHORUS (UV) ASSAY KIT

K Number: K862834 · Decision Aug 19, 1986
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
77
Review Days
25

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Basic Information

Device Name
MODEL 115-16 PHOSPHORUS (UV) ASSAY KIT
K Number
K862834
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Diagnostic Chemicals, Ltd. (Usa)
Date Received
July 25, 1986
Decision Date
August 19, 1986
Product Code
CEO
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
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus

Similar 510(k) Clearances

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

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Other Clearances by Diagnostic Chemicals, Ltd. (Usa)

K Number Device Name
K022538 IMMUNODIP URINARY ALBUMIN SCREEN ASSAY, CATALOGUE NUMBER 790-25
K974874 BILIRUBIN-SL (TOTAL) ASSAY
K932556 AMMONIA ASSAY CAT. NO. 200-02
K932766 HDL-CHOLESTRAL(DEXTRAN SULFATE/MAGNESIUM)
K932555 DC-LINEATE CAT. NO. SE-091
K925877 DC-UIBC-CAL
K912825 MAGNESIUM ASSAY KIT, CAT.# 100-12
K895964 DCL SYPHILIS-M CATALOG NO. 600-80
K895965 DCL - SYPHILIS-G ASSAY CATALOG NO. 600-70
K904660 ENZYMATIC BILIRUBIN (TOTAL), CATALOGUE NO. 202-14
Search all 77 clearances from Diagnostic Chemicals, Ltd. (Usa) →