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

CRIT-LINE HEMATOCRIT ALERT (MODIFICATION)

K Number: K953875 · Decision Jul 23, 1996
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
17
Applicant Total
8
Review Days
391

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Basic Information

Device Name
CRIT-LINE HEMATOCRIT ALERT (MODIFICATION)
K Number
K953875
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
In-Line Diagnostics Corp.
Date Received
June 28, 1995
Decision Date
July 23, 1996
Product Code
MQS
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
MQS System, Hemodialysis, Access Recirculation Monitoring

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Other Clearances by In-Line Diagnostics Corp.

K Number Device Name
K001763 CRIT-LINE MONITOR III (CLM III)
K992227 CRIT-LINE MONITOR III (CLM III)
K983551 CRIT-SCAN II MONITOR
K982412 MODIFICATION OF CRIT-LINE MONITOR III (CLM III)
K972470 CRIT-LINE MONITOR (CLMIII)
K950942 CRIT-LINE HEMATOCRIT ALERT
K935958 CRIT-LINE BLOOD CHAMBER WITH E-BEAM