PMA
P830028: UNISCEPT(TM)
FDA PMA · Manual antimicrobial susceptibility test systems · Analytical Products, Inc.
Key facts
| PMA number | P830028 |
|---|---|
| Trade name | UNISCEPT(TM) |
| Generic name | Manual antimicrobial susceptibility test systems |
| Applicant | Analytical Products, Inc. |
| Product code | JWY |
| Approval date | Mar 1, 1984 |
| Docket number | 84M-0129 |
| Notice date | Apr 25, 1984 |
At a glance
- 1–9 Supplements
- Mar 9, 1984 Latest supplement decision
- No Withdrawn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: