BURTON RADIUSGAUGE - MODEL 2030— 510(k) K924785
Substantially EquivalentR.H. Burton Co.
FDA 510(k) clearance K924785 for BURTON RADIUSGAUGE - MODEL 2030, Substantially Equivalent on 1993-04-05. Applicant: R.H. Burton Co..
Clearance details
- Applicant
- R.H. Burton Co.
- Product code
- Code HLM
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grove City, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.