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510(k) K833647

PACEMAKER SYS ANALYZER #384 by Pacesetter Systems — Product Code KRE

K833647 is an FDA 510(k) premarket notification submitted by Pacesetter Systems for the device "PACEMAKER SYS ANALYZER #384". The FDA issued a decision of Substantially Equivalent on December 16, 1983. The device falls under product code KRE (Analyzer, Pacemaker Generator Function, Indirect), a Class II device regulated under 21 CFR 870.3640. Pacesetter Systems has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 16, 1983
Date Received
October 17, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Pacemaker Generator Function, Indirect
Device Class
Class II
Regulation Number
870.3640
Review Panel
CV
Submission Type

Other clearances by Pacesetter Systems

  • K910924 — ENDOCARDIAL LEADS-MOD. TO THE POLYVINYLPYRROLIDONE (August 28, 1991)
  • K902147 — ENDOCARDIAL SCREW-IN LEAD MODEL 1028T (July 17, 1990)
  • K900512 — SIEMENS ELEMA MODELS 4020T AND 4021T ADAPTERS (June 25, 1990)
  • K900550 — FAST-PASS ACE MODELS 1212T/1222T/1216T/1226T (April 20, 1990)
  • K895447 — ENDOCARDIAL SCREW-IN LEAD MODEL 1020T (December 20, 1989)
  • K891905 — CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE (June 5, 1989)
  • K885267 — VS-1 MODEL NUMBER 251K PULSE GENERATOR (March 28, 1989)
  • K890547 — SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS (March 22, 1989)
  • K884733 — AFP MODEL 262T PULSE GENERATOR (February 10, 1989)
  • K883087 — PROLOG MP 658M PULSE GENERATOR (September 14, 1988)

Other clearances for product code KRE

  • K110693 — PACEART OPTIMA SYSTEM SOFTWARE (June 8, 2011)
  • K072950 — CYGNUS 12 LEAD ECG MODULE (August 22, 2008)
  • K032926 — EKG SPEAKS (October 15, 2003)
  • K922742 — HPM 40 HEART PACEMAKER MONITOR (March 18, 1993)
  • K915632 — PACEART CPTS-86/12 (April 14, 1992)
  • K895535 — PACEVIEW (March 19, 1990)
  • K870909 — PACEMAKER FUNCTION ANALYZER (April 27, 1987)
  • K832959 — PACEMAKER SYS. ANALYZER 378 (November 14, 1983)
  • K803286 — CARDIOMEMO (March 17, 1981)
  • K800696 — ELECTRONIC PACEMAKER WAVEFORM ANALYZER (August 14, 1980)

FDA data resources