Medical Device Manufacturer · US , Sylmar , CA

Minimed, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2000

Total

Cleared

Denied

Minimed, Inc. has 9 FDA 510(k) cleared medical devices. Based in Sylmar, US.

Historical record: 9 cleared submissions from 2000 to 2003. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Minimed, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Minimed, Inc.

9 devices

1-9 of 9

Cleared Nov 18, 2003

PARADIGMPAL, MODEL MMT-7330

K031541 · LZG

General Hospital · 186d

Cleared Jul 23, 2003

MEDTRONIC MINIMED PARADIGM INSULIN PUMP, MODEL MMT-712

K031390 · LGZ

General Hospital · 82d

Cleared Jun 17, 2003

MEDTRONIC MINIMED PARADIGM MODEL 512 INSULIN PUMP AND THE BD PARADIGM LINK...

K030531 · LZG

General Hospital · 118d

Cleared Aug 06, 2002

MEDTRONIC MINIMED COMLINK, HARDWARE MODEL 7304 & SOFTWARE MODEL 7311

K021974 · MRZ

General Hospital · 50d

Cleared Apr 05, 2001

MIMIMED SIL-SERTER INFUSION SET INSERTION SYSTEM, MODEL 385

K010377 · KZH

General Hospital · 56d

Cleared Aug 18, 2000

PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325

K001827 · FPA

General Hospital · 63d

Cleared Aug 18, 2000

PARADIGM 1.5ML RESERVOIR, MODEL 326

K001828 · FRN

General Hospital · 63d

Cleared Aug 18, 2000

MINIMED PARADIGM INSULIN PUMP, MODEL 511

K001829 · FRN

General Hospital · 63d

Cleared Aug 18, 2000

PARADIGM SOF-SET ULTIMATE QR, MODELS 317 AND 318

K001832 · FPA

General Hospital · 63d

Minimed, Inc. - FDA 510(k) Cleared Devices

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