510(k) K828605
K828605 is an FDA 510(k) premarket notification submitted by Rinn Corp. for the device "BEAM LIMITING DEVICE". The FDA issued a decision of Substantially Equivalent on January 3, 1983. Rinn Corp. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 3, 1983
- Date Received
- November 29, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No