TEST MAGNET— 510(k) K813153

Substantially Equivalent

Pacesetter Systems

FDA 510(k) clearance K813153 for TEST MAGNET, Substantially Equivalent on 1981-12-02. Applicant: Pacesetter Systems. Device class: 1.

Clearance details

Applicant: Pacesetter Systems
Product code: Code DTG
Device class: Class 1
Regulation: 21 CFR 870.3690
Advisory panel: Cardiovascular
Date received: 1981-11-06
Decision date: 1981-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DTG

K092364 — MODEL 220 PATIENT MAGNET2009-11-03
K960849 — MAGNO ALARM1997-03-26
K895110 — MAESTRO PACEMAKER TEST MAGNET1989-09-26
K831926 — IMPLANTABLE ENDOCARDIAL PACING LEADS1984-03-12

More clearances from Pacesetter Systems

K910924 — ENDOCARDIAL LEADS-MOD. TO THE POLYVINYLPYRROLIDONE1991-08-28
K902147 — ENDOCARDIAL SCREW-IN LEAD MODEL 1028T1990-07-17
K900512 — SIEMENS ELEMA MODELS 4020T AND 4021T ADAPTERS1990-06-25
K900550 — FAST-PASS ACE MODELS 1212T/1222T/1216T/1226T1990-04-20
K895447 — ENDOCARDIAL SCREW-IN LEAD MODEL 1020T1989-12-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.