PMA
P100020: COBAS HPV TEST
FDA PMA · KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS · Roche Molecular Systems, Inc.
Key facts
| PMA number | P100020 |
|---|---|
| Trade name | COBAS HPV TEST |
| Generic name | KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS |
| Applicant | Roche Molecular Systems, Inc. |
| Owner/operator | Roche Diagnostics Operations Inc. |
| Product code | MAQ |
| Approval date | Apr 19, 2011 |
| Docket number | 11M-0300 |
| Notice date | May 6, 2011 |
| Establishment registration | 2243471 |
| FEI number | 2243471 |
At a glance
- 10–99 Supplements
- Mar 17, 2026 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 10–99 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: