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

BION MUMPS-G ANTIBODY TEST SYSTEM

K Number: K926066 · Decision Jun 15, 1993
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
2
Applicant Total
14
Review Days
196

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Basic Information

Device Name
BION MUMPS-G ANTIBODY TEST SYSTEM
K Number
K926066
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2460
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bion Ent., Ltd.
Date Received
December 1, 1992
Decision Date
June 15, 1993
Product Code
CAR
Advisory Committee
General Hospital
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
CAR Monitor, Spinal-Fluid Pressure, Electrically Powered

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Other Clearances by Bion Ent., Ltd.

K Number Device Name
K901054 BION BORRELIA BURGDORFERI ANTIGEN SUBSTRATE SLIDE
K894622 VARICELLA ZOSTER VIRUS
K894624 MUMPS VIRUS
K894623 RESPIRATORY SYNCYTIAL VIRUS
K894626 EPSTEIN-BARR VIRUS-NUCLEAR ANTIGEN
K891785 BION EBV-G (VCA) TEST SYSTEM
K894625 CHLAMYDIA (LGV-1)
K893240 BION EBV-M (VCA) TEST SYSTEM
K890616 BION DIRECT IDENTIFICATION CONTROL SLIDE
K881261 BION HSV1-G OR HSV2-G TEST SYSTEM
Search all 14 clearances from Bion Ent., Ltd. →