The following data is part of a premarket notification filed by Surgical Instrument Service And Savings Inc (dba Medline Ren with the FDA for Livewire Electrophysiology Catheter.
Device ID | K151617 |
510k Number | K151617 |
Device Name: | Livewire Electrophysiology Catheter |
Classification | Catheter, Recording, Electrode, Reprocessed |
Applicant | SURGICAL INSTRUMENT SERVICE AND SAVINGS INC (DBA MEDLINE REN 2747 SW 6TH ST. Redmond, OR 97756 |
Contact | Brandi J. Panteleon |
Correspondent | Brandi J. Panteleon SURGICAL INSTRUMENT SERVICE AND SAVINGS INC (DBA MEDLINE REN 2747 SW 6TH ST Redmond, OR 97756 |
Product Code | NLH |
CFR Regulation Number | 870.1220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-06-15 |
Decision Date | 2016-01-22 |
Summary: | summary |