GDB — Endoscope, Fiber Optic Class II
FDA Device Classification
Classification Details
- Product Code
- GDB
- Device Class
- Class II
- Regulation Number
- 876.1500
- Submission Type
- Review Panel
- GU
- Medical Specialty
- Gastroenterology, Urology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K032283 | designs for vision | DESIGNS FOR VISION FIBEROPTIC LIGHT | August 20, 2003 |
| K961536 | matrix medica | FLEXSCOPE | September 18, 1996 |
| K935818 | cuda products | ENDOSCOPE | July 13, 1994 |
| K882061 | olympus | OLYMPUS GF-UM3/EU-M3 | November 15, 1988 |
| K855151 | regtec | FRITCH OPHTHALMIC ENDOSCOPE | February 19, 1986 |
| K843900 | medical diagnostics, ca | FOCUSCOPE UNIVERSAL SYSTEM | December 6, 1984 |
| K810007 | pentax precision instrument | PENTAX UPPER G.I. FIBERSCOPE, #FG-34 | January 15, 1981 |