The following data is part of a premarket notification filed by Oscor Inc. with the FDA for Permanent Pacing Leads, Models Physique Pb And Pjb.
Device ID | K024053 |
510k Number | K024053 |
Device Name: | PERMANENT PACING LEADS, MODELS PHYSIQUE PB AND PJB |
Classification | Permanent Pacemaker Electrode |
Applicant | Oscor Inc. 3816 DE SOTO BLVD. Palm Harbor, FL 34683 |
Contact | Mila Doskocil |
Correspondent | Mila Doskocil Oscor Inc. 3816 DE SOTO BLVD. Palm Harbor, FL 34683 |
Product Code | DTB |
CFR Regulation Number | 870.3680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-12-09 |
Decision Date | 2003-01-31 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
40836559009250 | K024053 | 000 |