ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT— 510(k) K970878
Substantially EquivalentAmerican Medical Devices, Inc.
FDA 510(k) clearance K970878 for ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT, Substantially Equivalent on 1997-05-06. Applicant: American Medical Devices, Inc..
Clearance details
- Applicant
- American Medical Devices, Inc.
- Product code
- Code MPA
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Atlanta, GA, US
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