VITROTEC TRUE LIGHT ENDOILLUMINATOR (100-S)— 510(k) K964555
Substantially EquivalentVitrotec, Inc.
FDA 510(k) clearance K964555 for VITROTEC TRUE LIGHT ENDOILLUMINATOR (100-S), Substantially Equivalent on 1997-03-31. Applicant: Vitrotec, Inc.. Device class: 2.
Clearance details
- Applicant
- Vitrotec, Inc.
- Product code
- Code MPA
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chesterfield, MO, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.