DISPOSABLE VACUUM CURETTE— 510(k) K790032

Name: FDA 510(k) clearance K790032
Creator: U.S. Food and Drug Administration
Published: 1979-02-01

Substantially Equivalent

British Marketing Ent., Ltd.

FDA 510(k) clearance K790032 for DISPOSABLE VACUUM CURETTE, Substantially Equivalent on 1979-02-01. Applicant: British Marketing Ent., Ltd.. Device class: 1.

Clearance details

Applicant: British Marketing Ent., Ltd.
Product code: Code HCY
Device class: Class 1
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1979-01-03
Decision date: 1979-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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