HEM-AVERT PERIANAL STABILIZER— 510(k) DEN090011
UnknownPlexus Biomedical, Inc.
FDA 510(k) clearance DEN090011 for HEM-AVERT PERIANAL STABILIZER, Unknown on 2011-01-13. Applicant: Plexus Biomedical, Inc.. Device class: 2.
Clearance details
- Applicant
- Plexus Biomedical, Inc.
- Product code
- Code OOA
- Device class
- Class 2
- Regulation
- 21 CFR 884.5200
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Oakland, TN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.