Richard-Allan Medical Ind., Inc.

FDA 510(k) & PMA Approved Devices — 33 products

Total Devices33

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K931879	REFLEX HTR	GCJ	1994-03-24	View
510(k)	K924200	REFLEX(R) ESC	KNF	1994-02-22	View
510(k)	K926297	REFLEX ESI	GEI	1993-10-15	View
510(k)	K924761	STERILE ENDOSCOPIC DISPOS TROCARS W/SAFE SHIELD	GCJ	1993-04-20	View
510(k)	K900566	RICHARD-ALLAN VESSEL LOOPS	KDC	1990-05-03	View
510(k)	K896262	TITANIUM LIGATING CLIPS	HBT	1990-01-02	View
510(k)	K890314	PROTECTOR (SURGICAL INSTRUMENT)	MMK	1989-02-27	View
510(k)	K873309	REFLEX(TM) CA-T CLIP APPLIER	FZP	1987-11-27	View
510(k)	K862404	REFLEX(TM) CLIP APPLIER	FZP	1986-07-23	View
510(k)	K862223	MICRO THIN* PARAFFIN	KEO	1986-06-17	View
510(k)	K861890	100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2	PPM	1986-06-03	View
510(k)	K832451	CLEAR-RITE 3	KEM	1983-08-12	View
510(k)	K830867	REFLEX ONE STAPLE EXTRACTOR		1983-04-12	View
510(k)	K830627	CLARIFIER-RICHARD-ALLAN	KEM	1983-03-24	View
510(k)	K830625	CYTO-STAIN	HJQ	1983-03-24	View
510(k)	K822145	COMPLETE	FZQ	1982-10-22	View
510(k)	K812847	XYLENE	KEM	1981-10-29	View
510(k)	K812846	CLEAR-RITE II	KEM	1981-10-29	View
510(k)	K811800	BLUING REAGENT	PPM	1981-08-12	View
510(k)	K811793	FIX-RIGHT 90ML & 180 ML PREFILLED CONT	KDT	1981-07-31	View