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BEAM LIMITING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K828605
510(k) Type
Traditional
Applicant
RINN CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1983
Days to Decision
35 days

BEAM LIMITING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K828605
510(k) Type
Traditional
Applicant
RINN CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1983
Days to Decision
35 days