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

ORTHO ABNORMAL COAGULATION LEVEL I/II

K Number: K832225 · Decision Aug 12, 1983
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
180
Applicant Total
126
Review Days
35

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Basic Information

Device Name
ORTHO ABNORMAL COAGULATION LEVEL I/II
K Number
K832225
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Ortho Diagnostic Systems, Inc.
Date Received
July 8, 1983
Decision Date
August 12, 1983
Product Code
JPA
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
JPA System, Multipurpose For In Vitro Coagulation Studies

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Other Clearances by Ortho Diagnostic Systems, Inc.

K Number Device Name
K951459 ORTHO-MUNE OKT 4A (CD4) - MONOCLONAL ANTIBODY (MURINE) FITC CONJUGATE
K951632 ORTHO-MUNE OK-COMBO CONTROL IGG2A-FITC/IGG2A-PE MONOCLONAL ANTIBODY (MURINE)
K964754 ORTHO-MUNE OKB (CD19)- MONOCLONAL ANTIBODY (MURINE) PHYCOERYTHRINE CONJUGATE
K963902 QUANTITATIVE FIBRINOGEN ASSAY
K950625 ORTHO-MUNE OK-COMBO CD40FITC/CD8-PE (OKT4A/OKT8) MONOCLONAL ANTIBODY (MURINE)
K951100 ORTHO-MUNE OK-COMBO CD3-FITC/CD19-PE (OKT3/OKB19A MONOLCLONAL ANTIBODY (MURINE)
K950568 ORTHO-MUNE OK-COMBO CD3-FITC/CD4-PE (OKT2/OKT4A) MONOCLONAL ANTIBODY (MURINE)
K950482 ORTHO-MUNE OK-COMVO CD3-FITC/CD8-PE (OKT 3/OKT8) MONOCLONAL ANTIBODY (MURINE)
K935720 ORTHO COUNT CALIBRATION KIT FOR ORTHO CYTORONABSOLUTE LASER FLOW CYTOMETRY SYSTEM
K954570 ORTHO IMMUNOCOUNT FLOW CYTOMETRY SYSTEM
Search all 126 clearances from Ortho Diagnostic Systems, Inc. →