Product code FBX
- Device name
- Sound, Urethral, Metal Or Plastic
- Medical specialty
- Gastroenterology, Urology
- Device class
- 1
- Regulation number
- 876.5520
- Review panel
- GU
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K950633 | CANDELA URETHRAL/BLADDER SOUND | Candela Laser Corp. | 1995-03-06 |
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