DISPOSABLE INTRAUTERINE PRESSURE KIT MODEL 13972A— 510(k) K885316
Substantially EquivalentHewlett-Packard Co.
FDA 510(k) clearance K885316 for DISPOSABLE INTRAUTERINE PRESSURE KIT MODEL 13972A, Substantially Equivalent on 1989-03-23. Applicant: Hewlett-Packard Co..
Clearance details
- Applicant
- Hewlett-Packard Co.
- Product code
- Code KXO
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andover, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.