VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER— 510(k) K827577
Substantially EquivalentRandwal Instrument Co., Inc.
FDA 510(k) clearance K827577 for VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER, Substantially Equivalent on 1983-01-24. Applicant: Randwal Instrument Co., Inc..
Clearance details
- Applicant
- Randwal Instrument Co., Inc.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Southbridge, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.