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

NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEM

K Number: K090696 · Decision Jun 19, 2009
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
20
Applicant Total
7
Review Days
95

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Basic Information

Device Name
NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEM
K Number
K090696
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Corventis, Inc.
Date Received
March 16, 2009
Decision Date
June 19, 2009
Product Code
QYX
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
QYX Outpatient Cardiac Telemetry

Similar 510(k) Clearances

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

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Other Clearances by Corventis, Inc.

K Number Device Name
K133701 NUVANT MCT SYSTEM
K113372 NUVANT, MOBILC CARDIAC TELEMETRY
K113187 AVIVO MOBILE PATIENT MANAGEMENT
K111917 NUVANT, MOBILE CARDIAC TELEMETRY
K091971 AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEM
K083287 AVIVO MOBILE PATIENT MANAGEMENT SYSTEM