ISOFLO AND ISOTEC INTRAUTERINE PRESSURE MONITORING— 510(k) K895763
Substantially EquivalentHealthdyne Cardiovascular, Inc.
FDA 510(k) clearance K895763 for ISOFLO AND ISOTEC INTRAUTERINE PRESSURE MONITORING, Substantially Equivalent on 1989-12-22. Applicant: Healthdyne Cardiovascular, Inc..
Clearance details
- Applicant
- Healthdyne Cardiovascular, Inc.
- Product code
- Code KXO
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Costa Mesa, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.