ENDOSCOPE— 510(k) K933106
Substantially EquivalentOrigin Medsystems, Inc.
FDA 510(k) clearance K933106 for ENDOSCOPE, Substantially Equivalent on 1993-10-19. Applicant: Origin Medsystems, Inc.. Device class: 2.
Clearance details
- Applicant
- Origin Medsystems, Inc.
- Product code
- Code ODF
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Menlo Park, CA, US
Recent devices under product code ODF
view all- K092739 — MICROENDOSCOPE MODEL S-0001 SINGLE LIGHT SOURCE, MICROENDOSCOPE, MODEL D-0001 DUAL LIGHT SOURCE STERILE
- K091962 — POLYSCOPE FLEXIBLE ENDOSCOPY CATHETER; 10,000 PIXEL FIBER OPTIC; XENON LIGHT SOURCE, MODEL LS-200
- K090170 — SPYSCOPE ACCESS AND DELIVERY CATHETER
- K052194 — SPYGLASS DIRECT VISUALIZATION PROBE AND OCULAR
- K050403 — SPYGLASS DIRECT VISULATION PROBE
More clearances from Origin Medsystems, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.