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

ELECSYS FERRITIN

K Number: K971833 · Decision Jun 2, 1997
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
23
Applicant Total
340
Review Days
14

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Basic Information

Device Name
ELECSYS FERRITIN
K Number
K971833
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5340
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Boehringer Mannheim Corp.
Date Received
May 19, 1997
Decision Date
June 2, 1997
Product Code
JMG
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
JMG Radioimmunoassay (Two-Site Solid Phase), Ferritin

Similar 510(k) Clearances

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Other Clearances by Boehringer Mannheim Corp.

K Number Device Name
K984326 ELECYS IGE ASSAY
K983047 ACCU-CHEK HQ SYSTEM
K984419 ELECSYS IGE CALCHECK
K984425 MODIFICATION OF PRECISET SERUM PROTEINS CALIBRATOR
K984372 ELECSYS CALCHECK TROPONIN T
K984105 ELECSYS TROPONIN T STAT TEST
K983503 ROCHE DIAGNOSTICS, BOEHRINGER MANNHEIM CORPORATION INORGANIC PHOSPHORUS REAGENT CATALOG NUMBER 1730347
K983469 PRECISET SERUM PROTEINS CALIBRATOR
K983185 BOEHRINGER MANNHEIM TINA-QUANT IGE TEST
K982949 ELECSYS PSA, MODEL 2010
Search all 340 clearances from Boehringer Mannheim Corp. →