TAPERED CERVICAL DILATOR— 510(k) K840381

Name: FDA 510(k) clearance K840381
Creator: U.S. Food and Drug Administration
Published: 1984-04-30

Substantially Equivalent

Intl. Medical Technologies, Inc.

FDA 510(k) clearance K840381 for TAPERED CERVICAL DILATOR, Substantially Equivalent on 1984-04-30. Applicant: Intl. Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Intl. Medical Technologies, Inc.
Product code: Code HHI
Device class: Class 2
Regulation: 21 CFR 884.5070
Advisory panel: Obstetrics/Gynecology
Date received: 1984-01-30
Decision date: 1984-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K840380 — UTERINE SOUND1984-04-30
K840382 — VACUUM ASPIRATION CATHETER1984-04-30
K840383 — MENSTRUAL ASPIRATION KIT1984-04-30
K840384 — DIAGNOSTIC DILATATION & MENSTRUAL KIT1984-04-30

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