PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE— 510(k) K881456

Name: FDA 510(k) clearance K881456
Creator: U.S. Food and Drug Administration
Published: 1988-10-14

Substantially Equivalent

Laboratoire Ccd C/O Washington Regulatory Services

FDA 510(k) clearance K881456 for PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE, Substantially Equivalent on 1988-10-14. Applicant: Laboratoire Ccd C/O Washington Regulatory Services. Device class: 2.

Clearance details

Applicant: Laboratoire Ccd C/O Washington Regulatory Services
Product code: Code HHK
Device class: Class 2
Regulation: 21 CFR 884.1175
Advisory panel: Obstetrics/Gynecology
Date received: 1988-04-06
Decision date: 1988-10-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ringoes, NJ, US

Download summary PDF View on FDA.gov ↗

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K881220 — ENDOCYTE, DISPOSABLE ENDOMETRIAL SAMPLER1988-06-14

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