RIGHT ARTERIAL CATHETER— 510(k) K822910
Substantially EquivalentQuinton, Inc.
FDA 510(k) clearance K822910 for RIGHT ARTERIAL CATHETER, Substantially Equivalent on 1982-11-29. Applicant: Quinton, Inc..
Clearance details
- Applicant
- Quinton, Inc.
- Product code
- Code LFJ
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bothell, WA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.