DUAL LUMEN TRANSCERIVICAL INTRAUTERINE KIT— 510(k) K920044

Substantially Equivalent

Telos 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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