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 |