STORZ FIBEROPTIC ENDO-ILLUMINATORS— 510(k) K896549
Substantially EquivalentStorz Instrument Co.
FDA 510(k) clearance K896549 for STORZ FIBEROPTIC ENDO-ILLUMINATORS, Substantially Equivalent on 1990-02-15. Applicant: Storz Instrument Co..
Clearance details
- Applicant
- Storz Instrument Co.
- Product code
- Code HBI
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Louis, MO, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.