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Genesis Industries, Inc.

FDA 510(k) & PMA Approved Devices — 17 products

Total Devices17

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K994361	ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULTURE PLATE, ESP WELL	MQK	2000-02-18	View
510(k)	K962828	EVERT-IT	HGY	1997-02-10	View
510(k)	K880377	NOVO VIVO MODEL #17140 AND #17135	GAA	1988-04-04	View
510(k)	K880376	NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP	GBS	1988-02-16	View
510(k)	K833290	C & B 40 PENTRO C & B40	EIS	1984-01-03	View
510(k)	K833287	SATIN CAST ECONOCAST	EIS	1984-01-03	View
510(k)	K833278	C & B 45	EIS	1983-12-29	View
510(k)	K833289	C & B 61 PENTRON C & B61	EIS	1983-12-29	View
510(k)	K833280	SUPRA AP CHOICE 83	EIS	1983-12-26	View
510(k)	K833285	RX IV PENTRON IV	EIS	1983-12-22	View
510(k)	K833288	C & B57 PENTRON C & B57	EIS	1983-12-20	View
510(k)	K833283	RX ORY PENTRON C & B	EIS	1983-11-28	View
510(k)	K833284	RX 41 PENTRON 41	EIS	1983-11-28	View
510(k)	K833281	RX D PENTRON	EIS	1983-11-28	View
510(k)	K833279	NATURELLE-LITE	EIS	1983-11-28	View
510(k)	K833286	RX SEG ECONOPLUS	EIS	1983-11-28	View
510(k)	K833282	RX NYSP PENTRON 60	EIS	1983-11-28	View

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