The following data is part of a premarket notification filed by Gulf Medical Fiberoptics with the FDA for Endoscopic Fiberoptic Cable.
| Device ID | K021931 |
| 510k Number | K021931 |
| Device Name: | ENDOSCOPIC FIBEROPTIC CABLE |
| Classification | Illuminator, Fiberoptic, Surgical Field |
| Applicant | GULF MEDICAL FIBEROPTICS 376 DOUGLAS RD. UNIT D Oldsmar, FL 34677 |
| Contact | Marcelino Afanador |
| Correspondent | Marcelino Afanador GULF MEDICAL FIBEROPTICS 376 DOUGLAS RD. UNIT D Oldsmar, FL 34677 |
| Product Code | HBI |
| CFR Regulation Number | 878.4580 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-06-12 |
| Decision Date | 2002-09-06 |