Interrad Medical, Inc. · Class I · Cleared Jul 9, 2019
| K-number | K180994 |
| Device name | SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F |
| Applicant | Interrad Medical, Inc. |
| Product code | KMK |
| Device class | Class I |
| Decision date | Jul 9, 2019 |
| Decision | Substantially Equivalent |
| Regulation | 880.5210 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov