INFLATION PRO II
Device Facts
| Record ID | K895836 |
|---|---|
| Device Name | INFLATION PRO II |
| Applicant | Baxter Healthcare Corp |
| Product Code | MAV · Cardiovascular |
| Decision Date | Dec 20, 1989 |
| 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.
