K231095
- 510(k) number
- K231095
- Device name
- Tamper Evident Cap
- Applicant
- International Medical Industries, Inc. FL · US
- Product code
- FMF — Syringe, Piston
- Decision date
- 2024-09-04
- Date received
- 2023-04-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K231095.pdf
Official FDA record: K231095
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.