CATHETER, ARTERIAL LINE— 510(k) K790083

Name: FDA 510(k) clearance K790083
Creator: U.S. Food and Drug Administration
Published: 1979-01-25

Substantially Equivalent

Namic

FDA 510(k) clearance K790083 for CATHETER, ARTERIAL LINE, Substantially Equivalent on 1979-01-25. Applicant: Namic. Device class: 2.

Clearance details

Applicant: Namic
Product code: Code DQY
Device class: Class 2
Regulation: 21 CFR 870.1250
Advisory panel: Cardiovascular
Date received: 1979-01-12
Decision date: 1979-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DQY

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K260559 — NHanceIT2026-08-14
K262392 — APRO 35 Swift Catheter2026-08-12
K261766 — CPS Locator 3D Plus Delivery Catheter2026-07-29
K262240 — SSPC NXT Delivery Catheter2026-07-29
K261825 — Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter2026-07-02

More clearances from Namic

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K953676 — BREEZE DIGITAL INFLATION DEVICE1996-03-29
K951722 — PERCEPTOR COMPENSATOR MORSE MANIFOLD1996-03-25
K921322 — MORSE ANESTHESIA MANIFOLD1993-07-09
K822100 — HIGH PRESSURE CONTRAST INJECTION LINE1982-08-24
K813549 — CONTINUOUS FLUSH DEVICE1982-01-12

Adverse events under product code DQY

product code DQY

Death: 464
Injury: 4,489
Malfunction: 13,721
Other: 2
Total: 18,676

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.