MORSE DT MANIFOLD— 510(k) K902472
Substantially EquivalentNorth American Instrument Corp.
FDA 510(k) clearance K902472 for MORSE DT MANIFOLD, Substantially Equivalent on 1990-08-23. Applicant: North American Instrument Corp.. Device class: 2.
Clearance details
- Applicant
- North American Instrument Corp.
- Product code
- Code DRS
- Device class
- Class 2
- Regulation
- 21 CFR 870.2850
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Glens Falls, NY, US
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- K163172 — HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer Kit
More clearances from North American Instrument Corp.
view allAdverse events under product code DRS
product code DRS- Death
- 8
- Malfunction
- 776
- Total
- 784
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K902472
K-number listed on FDA's recall record- Z-2141-2026 — Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure transducer
- Z-2142-2026 — Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducer
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K902472.
Data sourced from openFDA. This site is unofficial and independent of the FDA.