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

MODIFICATION TO: ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK W/SMART ALRAMS

K Number: K012171 · Decision Jul 24, 2001
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
116
Applicant Total
7
Review Days
12

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Basic Information

Device Name
MODIFICATION TO: ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK W/SMART ALRAMS
K Number
K012171
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Visicu, Inc.
Date Received
July 12, 2001
Decision Date
July 24, 2001
Product Code
MSX
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
MSX System, Network And Communication, Physiological Monitors

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MSX), ordered by most recent decision date.

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Other Clearances by Visicu, Inc.

K Number Device Name
K211046 eCareManager 4.5
K171322 eCareManager 4.1
K171029 eCareCoordinator
K153156 eCareManager 4.0.1
K141706 ECARE COORDINATOR (ECC)
K001972 ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK