The following data is part of a premarket notification filed by In-line Diagnostics Corp. with the FDA for Modification Of Crit-line Monitor Iii (clm Iii).
| Device ID | K982412 |
| 510k Number | K982412 |
| Device Name: | MODIFICATION OF CRIT-LINE MONITOR III (CLM III) |
| Classification | System, Hemodialysis, Access Recirculation Monitoring |
| Applicant | IN-LINE DIAGNOSTICS CORP. 117 WEST 200 SOUTH Farmington, UT 84025 |
| Contact | Matthew L Haynie |
| Correspondent | Matthew L Haynie IN-LINE DIAGNOSTICS CORP. 117 WEST 200 SOUTH Farmington, UT 84025 |
| Product Code | MQS |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-07-13 |
| Decision Date | 1998-10-09 |
| Summary: | summary |