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

CHRONOCOR VI MODEL 5012

K Number: K915364 · Decision Feb 7, 1992
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
64
Applicant Total
18
Review Days
72

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Basic Information

Device Name
CHRONOCOR VI MODEL 5012
K Number
K915364
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3600
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Seamed Corp.
Date Received
November 27, 1991
Decision Date
February 7, 1992
Product Code
DTE
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
DTE Pulse-Generator, Pacemaker, External

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Other Clearances by Seamed Corp.

K Number Device Name
K923398 CPI MODEL 2215
K912507 CPI MODEL 2215 & SEAMED MODEL 3400
K910223 CPI MODEL 2215/SEAMED MODEL 3400
K883930 SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY
K872551 SEAMED MODEL 3200
K863903 SEA MED MODEL 6000
K860462 SEAMED MODEL 3000
K854648 SEAMED MODEL 4000
K852746 EXTERNAL PACEMAKER TELECTRONICS TE200
K851900 SEA MED DDD PACING SYSTEM ANALYZER
Search all 18 clearances from Seamed Corp. →