K233653
- 510(k) number
- K233653
- Device name
- Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga (3269.M04-00)
- Applicant
- Peregrine Surgical, LLC PA · US
- Product code
- MPA — Endoilluminator
- Decision date
- 2024-08-05
- Date received
- 2023-11-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K233653.pdf
Official FDA record: K233653
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.