# K982999: Greiner Minicollect Edta Blood Collection Tube

- Pathway: 510(k) (Traditional)
- Applicant: Greiner Meditech, Inc.
- Decided: Oct 16, 1998 after 50 days
- Product code: JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection)
- Device class: 2
- Regulation: 21 CFR 862.1675
- 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 K940905 (1994). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K940905: Microtainer Brand Tube with Edta (K2), Bd Becton Dickinson Vacutainer Systems Preanalytic (1994) Summary page 1.

## Indications for use
To collect, transport, store, and evaluate capillary blood specimens for hematology and lead tests.

Source page: https://510kreport.com/device/K982999
Methodology: https://510kreport.com/methodology