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Rinn Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K932134
RINN UNIVERSAL COLLIMATOR
July 26, 1993
K913885
RINN E-Z CAPPER
December 13, 1991
K828605
BEAM LIMITING DEVICE
January 3, 1983
K813378
UNI-BITE DENTAL X-RAY FILM HOLDER
January 29, 1982
K772313
X-RAY CO-ORDINATOR
January 30, 1978