ULTRANS DISPOSABLE INTRAUTERINE— 510(k) K882224

Name: FDA 510(k) clearance K882224
Creator: U.S. Food and Drug Administration
Published: 1989-10-12

Substantially Equivalent

Telos Medical Corp.

FDA 510(k) clearance K882224 for ULTRANS DISPOSABLE INTRAUTERINE, Substantially Equivalent on 1989-10-12. Applicant: Telos Medical Corp.. Device class: 2.

Clearance details

Applicant: Telos Medical Corp.
Product code: Code HFN
Device class: Class 2
Regulation: 21 CFR 884.2700
Advisory panel: Obstetrics/Gynecology
Date received: 1988-05-26
Decision date: 1989-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Keene, CA, US

Download summary PDF View on FDA.gov ↗

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