PMA
P960044: NEEDLE-EASE TM 2501
FDA PMA · Sharps needle destruction device · Millenium Medical Supply, Inc.
Key facts
| PMA number | P960044 |
|---|---|
| Trade name | NEEDLE-EASE TM 2501 |
| Generic name | Sharps needle destruction device |
| Applicant | Millenium Medical Supply, Inc. |
| Product code | MTV |
| Approval date | Mar 6, 1997 |
| Docket number | 97M-0186 |
| Notice date | Jun 11, 1997 |
At a glance
- 1–9 Supplements
- Feb 11, 1998 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- No Withdrawn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: