DUAL LUMEN TRANSCERIVICAL INTRAUTERINE KIT— 510(k) K920044
Substantially EquivalentTelos Medical Corp.
FDA 510(k) clearance K920044 for DUAL LUMEN TRANSCERIVICAL INTRAUTERINE KIT, Substantially Equivalent on 1992-04-03. Applicant: Telos Medical Corp.. Device class: 2.
Clearance details
- Applicant
- Telos Medical Corp.
- Product code
- Code KXO
- Device class
- Class 2
- Regulation
- 21 CFR 884.2700
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Keene, CA, US
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More clearances from Telos Medical Corp.
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