510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K828605Substantially Equivalent

Beam Limiting Device

Rinn Corp., Elgin IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K828605 is the FDA 510(k) clearance record for BEAM LIMITING DEVICE, cleared for Rinn Corp. on . FDA records list 3 510(k) clearances for Rinn Corp., from to . As of , FDA records show no recalls naming K828605.

Clearance record

Decision date
Received
(35 days to decision)
Review panel
Unknown
Applicant
Rinn Corp. 1212 Abbott Dr., Elgin IL
Third party review
No