PERITONE DISPOSAL SHEATH - RUBBER AND VINYL— 510(k) K860552

Name: FDA 510(k) clearance K860552
Creator: U.S. Food and Drug Administration
Published: 1986-04-17

Substantially Equivalent

Laurie Ann Kaiser, Ph.D.

FDA 510(k) clearance K860552 for PERITONE DISPOSAL SHEATH - RUBBER AND VINYL, Substantially Equivalent on 1986-04-17. Applicant: Laurie Ann Kaiser, Ph.D.. Device class: 2.

Clearance details

Applicant: Laurie Ann Kaiser, Ph.D.
Product code: Code HIR
Device class: Class 2
Regulation: 21 CFR 884.1425
Advisory panel: Obstetrics/Gynecology
Date received: 1986-02-14
Decision date: 1986-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bellerose, NY, US

Download summary PDF View on FDA.gov ↗

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