# K910764: The Perceptor (TM) Stand Alone Transducer

- Pathway: 510(k) (Traditional)
- Applicant: North American Instrument Corp.
- Decided: Apr 22, 1991 after 81 days
- Product code: DRS (Transducer, Blood-Pressure, Extravascular)
- Device class: 2
- Regulation: 21 CFR 870.2850
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K974241: Scimed Informer Pressure Wire System (1998), 0 descendants of its own

## Recalls of this device
- Feb 12, 2025 · Class II · Z-1429-2025: The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.

Source page: https://510kreport.com/device/K910764
Methodology: https://510kreport.com/methodology