REFLEX(R) ESC— 510(k) K924200

Substantially Equivalent

Richard-Allan Medical Ind., Inc.

FDA 510(k) clearance K924200 for REFLEX(R) ESC, Substantially Equivalent on 1994-02-22. Applicant: Richard-Allan Medical Ind., Inc.. Device class: 2.

Clearance details

Applicant: Richard-Allan Medical Ind., Inc.
Product code: Product code KNF
Device class: Class 2
Regulation: 21 CFR 884.4160
Advisory panel: Obstetrics/Gynecology
Date received: 1992-08-20
Decision date: 1994-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richland, MI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Richard-Allan Medical Ind., Inc.

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K896262 — TITANIUM LIGATING CLIPS1990-01-02

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