The following data is part of a premarket notification filed by Medtronic Minimed with the FDA for Minimed Infusion Pump, Model Mmt-507.
Device ID | K960001 |
510k Number | K960001 |
Device Name: | MINIMED INFUSION PUMP, MODEL MMT-507 |
Classification | Pump, Infusion, Insulin |
Applicant | MEDTRONIC MINIMED 12744 SAN FERNANDO RD. Sylmar, CA 91342 |
Contact | D On |
Correspondent | D On MEDTRONIC MINIMED 12744 SAN FERNANDO RD. Sylmar, CA 91342 |
Product Code | LZG |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Se Subject To Tracking Reg (ST) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-01-02 |
Decision Date | 1996-04-30 |
Summary: | summary |