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Rudolph Beaver, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K883361ARTHRO-TRAC(TM)October 13, 1988
K875030OCU-1May 3, 1988
K862709MECHANICAL CYSTITOMEAugust 1, 1986
K860305BEAVER MICRO-GEM GAUGE BLOCKFebruary 12, 1986
K852828BEAVER R-K KNIFENovember 4, 1985
K853129BEAVER MULTIPURPOSE SAPPHIRE KNIFEAugust 6, 1985