PERINEOMETER & VAGINAL PROBE (BIOFEEDBACK MONITOR #20 AND VAGINAL PROBE)— 510(k) K970145
Substantially EquivalentBiosearch Medical Products, Inc.
FDA 510(k) clearance K970145 for PERINEOMETER & VAGINAL PROBE (BIOFEEDBACK MONITOR #20 AND VAGINAL PROBE), Substantially Equivalent on 1997-08-11. Applicant: Biosearch Medical Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Biosearch Medical Products, Inc.
- Product code
- Code HIR
- Device class
- Class 2
- Regulation
- 21 CFR 884.1425
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Somerville, NJ, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.