FDA 510(k) FDA class 2 Substantially Equivalent - Subject to Tracking Reg. 🇺🇸 United States

MINIMED 508 INSULIN PUMP

K Number: K990801 · Decision Jun 8, 1999
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
83
Applicant Total
48
Review Days
90

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Basic Information

Device Name
MINIMED 508 INSULIN PUMP
K Number
K990801
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent - Subject to Tracking Reg.
Applicant
Medtronic Minimed
Date Received
March 10, 1999
Decision Date
June 8, 1999
Product Code
LZG
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LZG Pump, Infusion, Insulin

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Other Clearances by Medtronic Minimed

K Number Device Name
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K242775 InPen System App (MMT-8060 (iOS), MMT-8061 (Android))
K241622 Extended Reservoir; MiniMed Reservoir
K160860 MiniMed Quick-serter
K120206 MEDTRONIC MINIMED PARADIGM INSULIN PUMPS
K100432 POLYFIN INFUSION SET, MODELS MMT-165, MMT-365, MMT-366, MMT-312S AND MMT-312L AND SOF-SET INFUSION SETS
K073356 PARADIGM INSULIN INFUSION PUMP, MODELS MMT-512, MMT-712, MMT-515 AND MMT-715
K053177 MEDTRONIC MINIMED PARADIGM INSULIN PUMP, MODEL MMT-712E
K052431 MEDTRONIC MINIMED LEAPFROG II INFUSION SET, MODELS MMT-801S1, MMT-801L1, MMT-801S2, MMT-801L2, MMT-803S1
Search all 48 clearances from Medtronic Minimed →