The following data is part of a premarket notification filed by Ascent Healthcare Solutions with the FDA for Reprocessed Electrophysiology Catheters.
| Device ID | K090323 |
| 510k Number | K090323 |
| Device Name: | REPROCESSED ELECTROPHYSIOLOGY CATHETERS |
| Classification | Catheter, Recording, Electrode, Reprocessed |
| Applicant | ASCENT HEALTHCARE SOLUTIONS 10232 SOUTH 51ST ST. Phoenix, AZ 85044 |
| Contact | Katie Bray |
| Correspondent | Katie Bray ASCENT HEALTHCARE SOLUTIONS 10232 SOUTH 51ST ST. Phoenix, AZ 85044 |
| Product Code | NLH |
| CFR Regulation Number | 870.1220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-02-09 |
| Decision Date | 2009-04-01 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00885825007850 | K090323 | 000 |
| 00885825007522 | K090323 | 000 |
| 00885825007539 | K090323 | 000 |
| 00885825007546 | K090323 | 000 |
| 00885825007553 | K090323 | 000 |
| 00885825007560 | K090323 | 000 |
| 00885825007577 | K090323 | 000 |
| 00885825007584 | K090323 | 000 |
| 00885825007591 | K090323 | 000 |
| 00885825007614 | K090323 | 000 |
| 00885825007621 | K090323 | 000 |
| 00885825007638 | K090323 | 000 |
| 00885825007645 | K090323 | 000 |
| 00885825007652 | K090323 | 000 |
| 00885825007669 | K090323 | 000 |
| 00885825007676 | K090323 | 000 |
| 00885825007010 | K090323 | 000 |