PMA
N17511: HYSKON (32% DEXTRAN 70)
FDA PMA · FLUID, HYSTEROSCOPY · Coopervision Surgical
Key facts
| PMA number | N17511 |
|---|---|
| Trade name | HYSKON (32% DEXTRAN 70) |
| Generic name | FLUID, HYSTEROSCOPY |
| Applicant | Coopervision Surgical |
| Owner/operator | COOPERSURGICAL, INC. |
| Product code | LTA |
| Approval date | Sep 15, 1975 |
| Establishment registration | 1216677 |
| FEI number | 1216677 |
At a glance
- 10–99 Supplements
- May 14, 2008 Latest supplement decision
- Yes Withdrawn
- No Summary of safety and effectiveness on file
- None UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: