# K902472: Morse DT Manifold

- Pathway: 510(k) (Traditional)
- Applicant: North American Instrument Corp.
- Decided: Aug 23, 1990 after 80 days
- Product code: DRS (Transducer, Blood-Pressure, Extravascular)
- Device class: 2
- Regulation: 21 CFR 870.2850
- Recalls of this device: 2 (2 Class I)
- 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.
1 of 1 device in its family (counting itself) has 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.

## Recalls of this device
- Mar 24, 2026 · Class I · Z-2142-2026: Medline has identified the presence of particulate within the fluid path of the Manifolds.
- Mar 24, 2026 · Class I · Z-2141-2026: Medline has identified the presence of particulate within the fluid path of the Manifolds.

Source page: https://510kreport.com/device/K902472
Methodology: https://510kreport.com/methodology