CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100— 510(k) K992606
Substantially EquivalentCanon USA, Inc.
FDA 510(k) clearance K992606 for CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100, Substantially Equivalent on 2000-06-21. Applicant: Canon USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Canon USA, Inc.
- Product code
- Code HLI
- Device class
- Class 2
- Regulation
- 21 CFR 886.1570
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lake Success, NY, US
Recent devices under product code HLI
view allMore clearances from Canon USA, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.