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Portlyn Corp.

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

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K970083	DYNABITE HOT GI BIOPSY FORCEPS	KGE	1997-06-17	View
510(k)	K951447	DYNABITE CARDIOVASCULAR BIOPSY FORCEPS	DWZ	1995-07-27	View
510(k)	K952391	DYNABITE UROLOGICAL FORCEPS	FCL	1995-06-01	View
510(k)	K944245	DYNABITE LAPAROSCOPIC FORCEPS	HET	1994-11-15	View
510(k)	K934506	DYNABITE HYSTEROSCOPIC FORCEPS	HET	1994-03-22	View
510(k)	K901300	BIOPSY FORCEPS	DWZ	1990-06-29	View
510(k)	K896147	BIOPSY FORCEP (NON-ELECTRIC)	FCL	1990-04-16	View
510(k)	K896146	BIOPSY FORCEPS, (NON-RIGID)	EOQ	1990-03-09	View

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