INTRAUTERINE CATHETER— 510(k) K861305
Substantially EquivalentRam Development
FDA 510(k) clearance K861305 for INTRAUTERINE CATHETER, Substantially Equivalent on 1986-12-11. Applicant: Ram Development.
Clearance details
- Applicant
- Ram Development
- Product code
- Code HDR
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Israel, IL
Data sourced from openFDA. This site is unofficial and independent of the FDA.