# K132040: Vial Connector 13MM Closed Collar

- Pathway: 510(k) (Special)
- Applicant: Medimop Medical Projects, Ltd.
- Decided: Jul 31, 2013 after 29 days
- Product code: LHI (Set, I.V. Fluid Transfer)
- Device class: 2
- Regulation: 21 CFR 880.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K963583 (1996). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K963583: Mixject Dispensing Pin/with Detachable Vial Holder/with Detachable Vial Holder and Preattached Needle, Medimop Medical Projects, Ltd. (1996) Summary page 1.
- K001293: Modification to Mixject Dispensing Pin/with Detachable Vial Holder/with Detachable Vial Holder and Pre-Attached Needle, Medimop Medical Projects, Ltd. (2000) Summary page 2.

## Indications for use
The proposed device is indicated for the transfer and mixing of drugs contained in a vial.

Source page: https://510kreport.com/device/K132040
Methodology: https://510kreport.com/methodology