BEAM LIMITING DEVICE— 510(k) K828605
Substantially EquivalentRinn Corp.
FDA 510(k) clearance K828605 for BEAM LIMITING DEVICE, Substantially Equivalent on 1983-01-03. Applicant: Rinn Corp..
Clearance details
- Applicant
- Rinn Corp.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Elgin, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.