The following data is part of a premarket notification filed by Alliance Medical Corp. with the FDA for Reprocessed Electrophysiology Catheters.
| Device ID | K061045 |
| 510k Number | K061045 |
| Device Name: | REPROCESSED ELECTROPHYSIOLOGY CATHETERS |
| Classification | Catheter, Recording, Electrode, Reprocessed |
| Applicant | ALLIANCE MEDICAL CORP. 10232 SOUTH 51ST ST. Phoenix, AZ 85044 |
| Contact | Elizabeth Renken |
| Correspondent | Elizabeth Renken ALLIANCE MEDICAL CORP. 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 | 2006-04-14 |
| Decision Date | 2006-08-31 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00885825011109 | K061045 | 000 |
| 00885825011093 | K061045 | 000 |
| 00885825011086 | K061045 | 000 |
| 00885825011079 | K061045 | 000 |
| 00885825011055 | K061045 | 000 |
| 00885825011048 | K061045 | 000 |