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G.W.B. Intl., Ltd.

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K955671	RITLENG BICAN.LACR.SETS/SELF THREAD. MONOKAS(CHG.IN STER.)	OKS	1996-03-06	View
510(k)	K954094	OPHTA SIL- PUNCTAL PLUGS (MODIFICATION)	LZU	1995-10-05	View
510(k)	K950569	OPHTA SIL {SELF-THREADING MONOKA (RITLENG TYPE)}	LZU	1995-03-14	View
510(k)	K940508	OPHTA SIL (RITLENG PROBE AND LACRIMAL INTUBATION SET)	OKS	1994-05-04	View
510(k)	K911110	OPHTA SIL(R), ENULCEATION/EVISCERATION IMPLANTS	HPZ	1991-06-18	View
510(k)	K911108	OPHTA SIL (R), PUNCTAL PLUGS AND INSERTERS	LZU	1991-05-13	View
510(k)	K911109	OPHTA SIL (R), LACHRYMAL INTUBATION SETS	OKS	1991-05-01	View
510(k)	K896029	DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20	IYO	1990-01-12	View

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