CONFOSCAN— 510(k) K971953
Substantially EquivalentTomey Corporation USA
FDA 510(k) clearance K971953 for CONFOSCAN, Substantially Equivalent on 1997-08-14. Applicant: Tomey Corporation USA. Device class: 2.
Clearance details
- Applicant
- Tomey Corporation USA
- Product code
- Code HJO
- Device class
- Class 2
- Regulation
- 21 CFR 886.1850
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cambridge, MA, US
Recent devices under product code HJO
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