# K071307: Invirolink  and Inviro Tip Blunt Cannulas, Model 130001, 130501, 140001, 140002, 140003

- Pathway: 510(k) (Traditional)
- Applicant: Inviro Medical Devices, Inc.
- Decided: Feb 12, 2008 after 279 days
- Product code: FMI (Needle, Hypodermic, Single Lumen)
- Device class: 2
- Regulation: 21 CFR 880.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K790472 (1979). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013087: Single Dose Dispensing Pin, Model 2201, Alaris Medical Systems, Inc. (2001) Summary page 2.

## Most influential descendants
- K083851: Inviroblunt Cannula with and Without EZ Wings, Models 120522 and 120022 (2009), 1 descendant of its own
- K202732: SOL-CARE IV Bag Safety Connector (2021), 0 descendants of its own

## Indications for use
The InviroLink and InviroLink w/EZ Wings Plastic Cannulas are used in conjunction with a syringe as an additive device for aspiration from multi-dose medicine vials or injection into I.V. Systems and pre-slit septurns covering injection sites.

Source page: https://510kreport.com/device/K071307
Methodology: https://510kreport.com/methodology