ENDOCERVICAL ASPIRATOR— 510(k) K812175

Name: FDA 510(k) clearance K812175
Creator: U.S. Food and Drug Administration
Published: 1981-09-21

Substantially Equivalent

Fertility Instrumentation, Inc.

FDA 510(k) clearance K812175 for ENDOCERVICAL ASPIRATOR, Substantially Equivalent on 1981-09-21. Applicant: Fertility Instrumentation, Inc.. Device class: 2.

Clearance details

Applicant: Fertility Instrumentation, Inc.
Product code: Code HFC
Device class: Class 2
Regulation: 21 CFR 884.1050
Advisory panel: Obstetrics/Gynecology
Date received: 1981-08-03
Decision date: 1981-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.