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Genesis Industries, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K994361ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULFebruary 18, 2000
K962828EVERT-ITFebruary 10, 1997
K880377NOVO VIVO MODEL #17140 AND #17135April 4, 1988
K880376NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAPFebruary 16, 1988
K833290C & B 40 PENTRO C & B40January 3, 1984
K833287SATIN CAST ECONOCASTJanuary 3, 1984
K833278C & B 45December 29, 1983
K833289C & B 61 PENTRON C & B61December 29, 1983
K833280SUPRA AP CHOICE 83December 26, 1983
K833285RX IV PENTRON IVDecember 22, 1983
K833288C & B57 PENTRON C & B57December 20, 1983
K833281RX D PENTRONNovember 28, 1983
K833284RX 41 PENTRON 41November 28, 1983
K833279NATURELLE-LITENovember 28, 1983
K833282RX NYSP PENTRON 60November 28, 1983
K833286RX SEG ECONOPLUSNovember 28, 1983
K833283RX ORY PENTRON C & BNovember 28, 1983