# K951722: Perceptor Compensator Morse Manifold

- Pathway: 510(k) (Traditional)
- Applicant: Namic
- Decided: Mar 25, 1996 after 346 days
- Product code: DRS (Transducer, Blood-Pressure, Extravascular)
- Device class: 2
- Regulation: 21 CFR 870.2850
- Recalls of this device: none
- 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. The FDA summary names its predicate without a number.
- (no number) MORSE® DT Manifold: named in the summary without a submission number
- (no number) Stand Alone Transducer: named in the summary without a submission number

## Most influential descendants
- K100319: Merit Manifold with Integrated Transducer, Model 203LTCHN-R; 503LTCHN-R; 203LTPHN-R,203LTCHWN-R; 503LTCHWN-R; 203L (2010), 0 descendants of its own

## Indications for use
Both devices are intended for invasive pressure monitoring, catheterization procedures, fluid delivery and/or blood access maintenance.

Source page: https://510kreport.com/device/K951722
Methodology: https://510kreport.com/methodology