GINRAM SPECUVAG, GINRAM SPECUVAG AS, GINRAM CUSCOVAG, MODELS 720101, 720102, 720103, 720179, 720227, 720043— 510(k) K991827

Name: FDA 510(k) clearance K991827
Creator: U.S. Food and Drug Administration
Published: 1999-07-19

Substantially Equivalent

Ri Mos. S.R.L.

FDA 510(k) clearance K991827 for GINRAM SPECUVAG, GINRAM SPECUVAG AS, GINRAM CUSCOVAG, MODELS 720101, 720102, 720103, 720179, 720227, 720043, Substantially Equivalent on 1999-07-19. Applicant: Ri Mos. S.R.L.. Device class: 2.

Clearance details

Applicant: Ri Mos. S.R.L.
Product code: Code HIB
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1999-05-28
Decision date: 1999-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, MA, US

Download summary PDF View on FDA.gov ↗

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