CERVICAL-VAGINAL SPATULA— 510(k) K761348

Name: FDA 510(k) clearance K761348
Creator: U.S. Food and Drug Administration
Published: 1977-01-18

Substantially Equivalent

Law Offices of Natter & Natter

FDA 510(k) clearance K761348 for CERVICAL-VAGINAL SPATULA, Substantially Equivalent on 1977-01-18. Applicant: Law Offices of Natter & Natter. Device class: 2.

Clearance details

Applicant: Law Offices of Natter & Natter
Product code: Code HHT
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1976-12-28
Decision date: 1977-01-18
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.