GYNASPYR VACUUM CURETTAGE UNIT— 510(k) K850312

Substantially Equivalent

Roseburg SA

FDA 510(k) clearance K850312 for GYNASPYR VACUUM CURETTAGE UNIT, Substantially Equivalent on 1985-02-28. Applicant: Roseburg SA. Device class: 2.

Clearance details

Applicant: Roseburg SA
Product code: Code HHI
Device class: Class 2
Regulation: 21 CFR 884.5070
Advisory panel: Obstetrics/Gynecology
Date received: 1985-01-25
Decision date: 1985-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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More clearances from Roseburg SA

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K885275 — ASSENAT-BLESCHET SUNGLASSES1989-01-24
K882392 — BURNET LABORATOIRE PHARMACEUTIQUE SURGICAL GLOVES1988-08-26
K872715 — UNIVERSAL INSTRUMENTATION(CD) FOR SPINAL SURGERY1987-12-07

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