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

CAMBRIDGE HEART OEM

K Number: K100362 · Decision Apr 14, 2010
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
403
Applicant Total
17
Review Days
61

Basic Information

Device Name
CAMBRIDGE HEART OEM
K Number
K100362
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1425
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CAMBRIDGE HEART, INC.
Date Received
February 12, 2010
Decision Date
April 14, 2010
Product Code
DQK
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
DQK Computer, Diagnostic, Programmable

Similar 510(k) Clearances

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

View all

Other Clearances by CAMBRIDGE HEART, INC.

K Number Device Name
K050225 HEARTWAVE II CARDIAC DIAGNOSTIC SYSTEM
K022149 CARDIAC DIAGNOSTIC SYSTEM, MODEL CH2000
K022152 HEARTWAVE ALTERNANS PROCESSING SYSTEM, MODEL APS
K013565 CARDIAC DIAGNOSTIC SYSTEM, MODEL CH2000
K013564 MODIFICATION TO HEARTWAVE ALTERNANS PROCESSING SYSTEM, MODEL APS
K012206 ALTERNANAS PROCESSING SYSTEM, CH 2000 CARDIAC DIAGNOSTIC SYSTEM, HEARTWAVE ALTERNANS PROCESSING SYSTEM
K011324 CAMBRIDGE HEART MODEL CH 2000 CARDIAC DIAGNOSTIC SYSTEM
K010758 HEARTWAVE ALTERNANS PROCESSING SYSTEM, APS
K010756 CH 2000 CARDIAC DIAGNOSTIC SYSTEM
K003492 ANALYTIC SPECTRAL METHOD OF ALTERNANS PROCESSING; CH 2000 CARDIAC DIAGNOSTIC SYSTEM; HEARTWAVE ALTERNANS PROCESSING SYS
Search all 17 clearances from CAMBRIDGE HEART, INC. →