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 |