# K950830: Sta-Put Non-Magnetic Instrument Drape Catalog #100-187-00 (16X20), 100-186-00 (16X10), 100-183-00 W/Dexter Wrap

- Pathway: 510(k) (Traditional)
- Applicant: Avail-Southwest Division
- Decided: May 3, 1995 after 68 days
- Product code: KKX (Drape, Surgical, Antimicrobial)
- Device class: 2
- Regulation: 21 CFR 878.4370
- 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Source page: https://510kreport.com/device/K950830
Methodology: https://510kreport.com/methodology