7.5 MHZ ENDOVAGINAL PROBE— 510(k) K870709
Substantially EquivalentPhilips Ultrasound, Inc.
FDA 510(k) clearance K870709 for 7.5 MHZ ENDOVAGINAL PROBE, Substantially Equivalent on 1987-03-27. Applicant: Philips Ultrasound, Inc..
Clearance details
- Applicant
- Philips Ultrasound, Inc.
- Product code
- Code HGL
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Ana, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.