← Back to catalogue
BSC, SONICATH ULTRA IMAGING CATHETER 3.2F/20MHZ - Sonicath Ultra Imaging Catheter 2.9f
FDA 510(k)Class II (US FDA 510(k))
510(k) K970049
Identifiers
- 510(k) Number
- K970049 FDA 510(k)
- FDA Product Code
- ITX FDA 510(k)
- Models / Variants
- 37410 FDA 510(k)456221 & Bsc FDA 510(k)Sonicath Ultra Imaging Catheter 2.9f FDA 510(k)20mhz FDA 510(k)37411 FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 892.1570 FDA 510(k)
- Regulation Number
- 892.1570 FDA 510(k)
- Advisory Committee
- Radiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
BSC, SONICATH ULTRA IMAGING CATHETER 3.2F/20MHZ - Sonicath Ultra Imaging Catheter 2.9f by Cardiovascular Imaging Systems, Inc. — Class II — FDA_510K — listed…
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K970049 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Cardiovascular Imaging Systems, Inc.
Sources (1)
- FDA 510(k) K970049 24 fields · synced Jun 18, 2026