OMNITRON GYN APPLICATOR SYSTEM— 510(k) K913908
Substantially EquivalentOmnitron Intl., Inc.
FDA 510(k) clearance K913908 for OMNITRON GYN APPLICATOR SYSTEM, Substantially Equivalent on 1992-03-06. Applicant: Omnitron Intl., Inc.. Device class: 2.
Clearance details
- Applicant
- Omnitron Intl., Inc.
- Product code
- Code JAQ
- Device class
- Class 2
- Regulation
- 21 CFR 892.5700
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
Recent devices under product code JAQ
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