# K830221: Bedside N.P.T. 9900 - Printer 9800

- Pathway: 510(k) (Traditional)
- Applicant: Browne Medical, Inc.
- Decided: Mar 17, 1983 after 52 days
- Product code: LIL (Monitor, Penile Tumescence)
- Device class: U
- 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 has not posted a summary or statement for it, so its predicates are not known.

Source page: https://510kreport.com/device/K830221
Methodology: https://510kreport.com/methodology
