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

IMMULITE VITAMIN B12 (LKVB1,LKVB5)

K Number: K971177 · Decision May 16, 1997
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
77
Applicant Total
321
Review Days
46

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Basic Information

Device Name
IMMULITE VITAMIN B12 (LKVB1,LKVB5)
K Number
K971177
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1810
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diagnostic Products Corp.
Date Received
March 31, 1997
Decision Date
May 16, 1997
Product Code
CDD
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
CDD Radioassay, Vitamin B12

Similar 510(k) Clearances

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

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Other Clearances by Diagnostic Products Corp.

K Number Device Name
K063045 IMMULITE 2000, IMMULITE 2500 VANCOMYCIN
K034055 IMMULITE 2500 CK-MB, 2500 MYOGLOBIN, 2500 STAT TROPONIN I
K033234 IMMULITE 2500 AUTOMATED IMMUNOASSAY ANALYZER
K032881 IMMULITE/IMMULITE 1000 TOTAL TESTOSTERONE AND IMMULITE 2000 TOTAL TESTOSTERONE
K023152 IMMULITE 2000 ALLERGEN-SPECIFIC IGE
K023304 IMMULITE/IMMULITE 1000 CALCITONIN, MODEL LKCL AND IMMULITE 2000 CALCITONIN, MODEL L2KCL
K022603 IMMULITE 1000 AUTOMATED IMMUNOASSAY ANALYZER
K022118 IMMULITE TURBO CK-MB, MODELS LSKCP1 (100 TESTS), LSKCP5 (500 TESTS)
K021257 ANA LINE BLOT, CATALOG NUMBER: KALABI (20 TESTS)
K021208 IMMULITE 2000 MIXED ALLERGEN PANELS
Search all 321 clearances from Diagnostic Products Corp. →