# K990371: Diabetic Needle Disposal, Model # PMSM - 950

- Pathway: 510(k) (Traditional)
- Applicant: Post Medical, Inc.
- Decided: Apr 21, 1999 after 72 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Diabetic Disposal (D.N.D.) is to be used by the diabetic patient at home for the collection of contaminated disposable sharps at the point of use.

Source page: https://510kreport.com/device/K990371
Methodology: https://510kreport.com/methodology