510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K070438Substantially Equivalent

Medtronic Minimed Carelink Usb Connector, Model Nmt 7305

Medtronic, Inc., Northridge CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K070438 is the FDA 510(k) clearance record for MEDTRONIC MINIMED CARELINK USB CONNECTOR, MODEL NMT 7305, a class II device, cleared for Medtronic Minimed, Inc. on under FDA product code MRZ (Accessories, Pump, Infusion). FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K070438.

Clearance record

Decision date
Received
(244 days to decision)
Product code
MRZ Accessories, Pump, Infusion
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Medtronic Minimed, Inc. 18000 Devonshire St., Northridge CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MRZ

Trailing 12 months

FDA records hold no clearances under product code MRZ in the trailing twelve months.

FDA records show no clearances under product code MRZ in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MRZ, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260