HP MODEL M1318A TRANSVAGINAL ULTRASOUND TRANSDUCER— 510(k) K895026
Substantially EquivalentHewlett-Packard Co.
FDA 510(k) clearance K895026 for HP MODEL M1318A TRANSVAGINAL ULTRASOUND TRANSDUCER, Substantially Equivalent on 1989-11-06. Applicant: Hewlett-Packard Co.. Device class: 2.
Clearance details
- Applicant
- Hewlett-Packard Co.
- Product code
- Code HGL
- Device class
- Class 2
- Regulation
- 21 CFR 884.2960
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andover, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.