Focus T41,T41F,T43, T43F,T44F

FDA 510(k) K904255 · Elamedical

Substantially Equivalent

510(k) numberK904255

Submission

Device name
Focus T41,T41F,T43, T43F,T44F
Applicant
Elamedical
Minnetonka, MN, US
Received
September 17, 1990
Decision date
January 18, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DTB – Permanent Pacemaker Electrode
Device class
Class III (high risk)
Regulation
21 CFR 870.3680
Specialty
Cardiovascular
Implant
Yes

Other 510(k)s with product code DTB

510(k)DeviceApplicantDecision
K061212Biotronik Endocardial Pacing LeadsDTB · Special Biotronik, Inc.07/10/2006SE
K041809Permanent Pacing Lead, Model PY2DTB · Special Oscor, Inc.08/06/2004SE
K040569Permanent Pacing Lead, Model Refino, Model: Refino-R, Ru, RjuDTB · Special Oscor, Inc.04/07/2004SE
K031274Model 5071 Myocardial Pacing LeadDTB · Special Medtronic Vascular05/22/2003ST
K031210Model 4951M Myocardial Unipolar LeadDTB · Special Metronic, Inc.05/16/2003SE
K023205Elox P 45-BP; Elox P 53-BP; Elox P 60-BPDTB · Traditional Biotronik, Inc.04/24/2003ST
K024053Permanent Pacing Leads, Models Physique PB and PJBDTB · Special Oscor, Inc.01/31/2003SE
K023803Modification to Biotronik's Sterilization ProcessDTB · Special Biotronik, Inc.12/11/2002SE
K023099Arox 45-JBP; Arox 53-JBP; Merox 45-JBP; Merox 53-JBPDTB · Special Biotronik, Inc.10/18/2002SE
K021217Arox 53-BP; Arox 60-BP; Arox 45-JBP; Arox 53-JBPDTB · Special Biotronik, Inc.05/01/2002SE

Questions and answers

When was Focus T41,T41F,T43, T43F,T44F cleared by the FDA?

Focus T41,T41F,T43, T43F,T44F (K904255) received a 510(k) decision of Substantially Equivalent on January 18, 1991, 123 days after the submission was received.

What is the product code of K904255?

The FDA product code is DTB – Permanent Pacemaker Electrode, a Class III (high risk) device regulated under 21 CFR 870.3680.