# K852607: Monject Sterile 20CC Syringes

- Pathway: 510(k) (Traditional)
- Applicant: Sherwood Medical Co.
- Decided: Jul 23, 1985 after 34 days
- Product code: FMF (Syringe, Piston)
- Device class: 2
- Regulation: 21 CFR 880.5860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

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

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K983122: Mill-Rose Laboratories Transbronchial Needle Aspiration (Tbna) Combination Cytology/Histology Procedural Kit (1998), 0 descendants of its own
- K983124: Mill-Rose Laboratories Transbronchial Needle Aspiration (Tbna) Cytology Procedural Kit (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K852607
Methodology: https://510kreport.com/methodology