NEEDLES USED IN ANGIOGRAPHIC PROCED.— 510(k) K772369

Substantially Equivalent

Argon Medical Corp.

FDA 510(k) clearance K772369 for NEEDLES USED IN ANGIOGRAPHIC PROCED., Substantially Equivalent on 1978-01-24. Applicant: Argon Medical Corp..

Clearance details

Applicant: Argon Medical Corp.
Product code: Code DRC
Advisory panel: Cardiovascular
Date received: 1977-12-27
Decision date: 1978-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DRC

product code DRC

Death: 28
Injury: 412
Total: 440

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.