# K993012: Minimed Com-Station, Hardware-7301; Software-7311

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic Minimed
- Decided: Nov 15, 1999 after 68 days
- Product code: LZG (Pump, Infusion, Insulin)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Disetronic D-Modem: named in the summary without a submission number

## Most influential descendants
- K243774: ELID (Endoscopic Less Invasive Decompression) System (2025), 1 descendant of its own
- K252546: VantageTM Lumbar Decompression Kit (2026), 0 descendants of its own
- K020655: Deltec Insulin Infusion Pump and Accessories (2002), 0 descendants of its own

## Indications for use
The MiniMed Com-Station Communication System is indicated for use as an accessory to MiniMed infusion pumps (models 507, S07C, and 508), and LifeScan (One Touch) and Roche (Accu-Chek) blood glucose meters to transmit and display data from device memory banks.

Source page: https://510kreport.com/device/K993012
Methodology: https://510kreport.com/methodology