Medical Device Manufacturer · US , Anaheim , CA

Medtronic Blood Systems, Inc. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1988

Total

Cleared

Denied

Medtronic Blood Systems, Inc. has 15 FDA 510(k) cleared cardiovascular devices. Based in Anaheim, US.

Historical record: 15 cleared submissions from 1988 to 1995.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medtronic Blood Systems, Inc.

15 devices

1-12 of 15

Cleared Jul 14, 1995

TEMPORARY MYOCARDIAL PACING LEAD, MODEL 6500

K944957 · LDF

Cardiovascular · 280d

Cleared Jul 14, 1995

UNIPOLAR ATRIAL TEMPORARY PACING LEAD,MODEL 6492

K944966 · LDF

Cardiovascular · 276d

Cleared Dec 12, 1989

CLOSED CHEST SUPPORT CIRCUIT

K893207 · DTZ

Cardiovascular · 230d

Cleared Nov 27, 1989

DURAN FLEXIBLE ANNULOPLASTY RING & OBTURATOR H601H

K893678 · KRH

Cardiovascular · 195d

Cleared May 31, 1989

EXTRACORPOREAL CIRCUIT WITH BIO-ACTIVE SURFACE

K891687 · DTZ

Cardiovascular · 70d

Cleared May 19, 1989

MAXIMA* HOLLOW FIBER OXYGENATOR W/FILTERED RESERV.

K891230 · DTZ

Cardiovascular · 73d

Cleared Feb 22, 1989

INTERSEPT* CRYSTALLOID CARDIOPLEGIA DELIV. SYSTEM

K885154 · KRJ

Cardiovascular · 69d

Cleared Dec 21, 1988

INTERSEPT* CRYSTALLOID CARDIOPLEGIA FILTER

K884390 · KRJ

Cardiovascular · 64d

Cleared Dec 05, 1988

INTERSEPT* PREBYPASS FILTER

K884244 · KRJ

Cardiovascular · 55d

Cleared Oct 13, 1988

INTERSEPT*CRYSTALLOID CARDIOPLEGIA DELIVERY SYSTEM

K883439 · DTR

Cardiovascular · 59d

Cleared Sep 16, 1988

INTERSEPT*PREBYPASS FILTER

K883086 · KRJ

Cardiovascular · 57d

Cleared Aug 12, 1988

EXTENDED SHELF LIFE FOR INTERSEPT* ARTERIAL 20/40

K882137 · DTM

Cardiovascular · 84d

Medtronic Blood Systems, Inc. - FDA 510(k) Cleared Devices

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