PMA
P870062: PRENTIF TM CAVITY RIM CERVICAL CAP
FDA PMA · Cap, cervical, contraceptive · Lamberts Dalston, Ltd.
Key facts
| PMA number | P870062 |
|---|---|
| Trade name | PRENTIF TM CAVITY RIM CERVICAL CAP |
| Generic name | Cap, cervical, contraceptive |
| Applicant | Lamberts Dalston , Ltd. |
| Product code | LLQ |
| Approval date | May 23, 1988 |
| Docket number | 88M-0212 |
| Notice date | Jul 19, 1988 |
At a glance
- 1–9 Supplements
- Aug 20, 1991 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- No Withdrawn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: