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

IMMULITE 2000 3RD GENERATION PSA

K Number: K974842 · Decision Apr 21, 1998
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
32
Applicant Total
321
Review Days
118

Basic Information

Device Name
IMMULITE 2000 3RD GENERATION PSA
K Number
K974842
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.6010
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
DIAGNOSTIC PRODUCTS CORP.
Date Received
December 24, 1997
Decision Date
April 21, 1998
Product Code
LTJ
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LTJ Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

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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)
K021206 IMMULITE 2000 SPECIFIC ALLERGENS
Search all 321 clearances from DIAGNOSTIC PRODUCTS CORP. →