Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Medtronic Blood Systems, Inc.

FDA 510(k) & PMA Approved Devices — 15 products

Total Devices15

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K944966	UNIPOLAR ATRIAL TEMPORARY PACING LEAD,MODEL 6492	LDF	1995-07-14	View
510(k)	K944957	TEMPORARY MYOCARDIAL PACING LEAD, MODEL 6500	LDF	1995-07-14	View
510(k)	K893207	CLOSED CHEST SUPPORT CIRCUIT	DTZ	1989-12-12	View
510(k)	K893678	DURAN FLEXIBLE ANNULOPLASTY RING & OBTURATOR H601H	KRH	1989-11-27	View
510(k)	K891687	EXTRACORPOREAL CIRCUIT WITH BIO-ACTIVE SURFACE	DTZ	1989-05-31	View
510(k)	K891230	MAXIMA* HOLLOW FIBER OXYGENATOR W/FILTERED RESERV.	DTZ	1989-05-19	View
510(k)	K885154	INTERSEPT* CRYSTALLOID CARDIOPLEGIA DELIV. SYSTEM	KRJ	1989-02-22	View
510(k)	K884390	INTERSEPT* CRYSTALLOID CARDIOPLEGIA FILTER	KRJ	1988-12-21	View
510(k)	K884244	INTERSEPT* PREBYPASS FILTER	KRJ	1988-12-05	View
510(k)	K883439	INTERSEPT*CRYSTALLOID CARDIOPLEGIA DELIVERY SYSTEM	DTR	1988-10-13	View
510(k)	K883086	INTERSEPT*PREBYPASS FILTER	KRJ	1988-09-16	View
510(k)	K882137	EXTENDED SHELF LIFE FOR INTERSEPT* ARTERIAL 20/40	DTM	1988-08-12	View
510(k)	K882136	INTERSEPT* OXYGEN GAS LINE FILTER	KRD	1988-08-11	View
510(k)	K882479	26MM DIAMETER HANCOCK* TROCAR BLADE AND TIP	DWS	1988-07-18	View
510(k)	K880671	MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER	DTM	1988-05-06	View

↑