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..
Clearance details
- Applicant
- Telos Medical Corp.
- Product code
- Code KXO
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Keene, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.