FDA Product Code
FDA Product Code GDB — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Gastroenterology, Urology
- 21 CFR Citation
- 876.1500
510(k) Clearances — 7 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K032283 | DESIGNS FOR VISION FIBEROPTIC LIGHT | Designs For Vision, Inc. | 2003-08-20 | Special | PDF ↗ |
| K961536 | FLEXSCOPE | Matrix Medica, Inc. | 1996-09-18 | Traditional | PDF ↗ |
| K935818 | ENDOSCOPE | Cuda Products Co. | 1994-07-13 | Traditional | PDF ↗ |
| K882061 | OLYMPUS GF-UM3/EU-M3 | Olympus Corp. | 1988-11-15 | Traditional | PDF ↗ |
| K855151 | FRITCH OPHTHALMIC ENDOSCOPE | Regtec | 1986-02-19 | Traditional | PDF ↗ |
| K843900 | FOCUSCOPE UNIVERSAL SYSTEM | Medical Diagnostics, Ca. | 1984-12-06 | Traditional | PDF ↗ |
| K810007 | PENTAX UPPER G.I. FIBERSCOPE, #FG-34 | Pentax Precision Instrument Corp. | 1981-01-15 | Traditional | PDF ↗ |
Product code GDB · Class II · Gastroenterology, Urology. Data: openFDA.