FDA 510(k) Applications for Medical Device Product Code "FDG"
(Retractor, Fiberoptic)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K964561 | BIOENTERICS CORP. | ENDOLUMINA II TRANSILLUMINATION SYSTEM 56FR E-5630, 50FR E-5030 AND 40FR E-4020, ENDOLUMINA II DETACHABLE TIPS, 56FR, TA | 02/11/1997 |
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