The following data is part of a premarket notification filed by Siemens-pacesetter, Inc. with the FDA for Pacing Lead Model 1188t.
Device ID | K925038 |
510k Number | K925038 |
Device Name: | PACING LEAD MODEL 1188T |
Classification | Permanent Pacemaker Electrode |
Applicant | SIEMENS-PACESETTER, INC. 15900 VALLEY VIEW COURT P.O.BOX 9221 Sylmar, CA 91392 -9221 |
Contact | Nestor Kusnierz |
Correspondent | Nestor Kusnierz SIEMENS-PACESETTER, INC. 15900 VALLEY VIEW COURT P.O.BOX 9221 Sylmar, CA 91392 -9221 |
Product Code | DTB |
CFR Regulation Number | 870.3680 [🔎] |
Decision | Se Subject To Tracking Reg (ST) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-10-05 |
Decision Date | 1994-07-15 |