VERTEX MONITORING CATHETER
Device Facts
| Record ID | K823253 |
|---|---|
| Device Name | VERTEX MONITORING CATHETER |
| Applicant | Vertex Medical Corp. |
| Product Code | DXT · Cardiovascular |
| Decision Date | Dec 30, 1982 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 870.1650 |
| Device Class | Class 2 |
Regulatory Classification
Special Controls
*Classification.* Class II (special controls). The device, when it is a non-patient contacting balloon inflation syringe intended only to inflate/deflate balloon catheters and monitor pressure within the balloon, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 870.9.
