ARGON DUAL LUMEN HEMODIALYSIS, CATHETER— 510(k) K842039
Substantially EquivalentArgon Medical Corp.
FDA 510(k) clearance K842039 for ARGON DUAL LUMEN HEMODIALYSIS, CATHETER, Substantially Equivalent on 1985-01-29. Applicant: Argon Medical Corp..
Clearance details
- Applicant
- Argon Medical Corp.
- Product code
- Code KNZ
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Athens, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.