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

SEAMED MODEL 6000

K Number: K843807 · Decision Feb 1, 1985
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
64
Applicant Total
18
Review Days
127

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SEAMED MODEL 6000
K Number
K843807
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3600
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Seamed Corp.
Date Received
September 27, 1984
Decision Date
February 1, 1985
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

Similar 510(k) Clearances

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

View all

Other Clearances by Seamed Corp.

K Number Device Name
K923398 CPI MODEL 2215
K915364 CHRONOCOR VI MODEL 5012
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
Search all 18 clearances from Seamed Corp. →