The following data is part of a premarket notification filed by Stryker Sustainability Solutions with the FDA for Reprocessed Electrophysiology Catheters.
Device ID | K112232 |
510k Number | K112232 |
Device Name: | REPROCESSED ELECTROPHYSIOLOGY CATHETERS |
Classification | Catheter, Recording, Electrode, Reprocessed |
Applicant | STRYKER SUSTAINABILITY SOLUTIONS 1810 W. Drake Dr. Tempe, AZ 85283 |
Contact | Amanda Babcock |
Correspondent | Amanda Babcock STRYKER SUSTAINABILITY SOLUTIONS 1810 W. Drake Dr. Tempe, AZ 85283 |
Product Code | NLH |
CFR Regulation Number | 870.1220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-08-04 |
Decision Date | 2011-09-26 |
Summary: | summary |