LABOR/DELIVERY/RECOVERY BED LDR-600— 510(k) K833321

Name: FDA 510(k) clearance K833321
Creator: U.S. Food and Drug Administration
Published: 1983-11-14

Substantially Equivalent

Adel Medical , Ltd.

FDA 510(k) clearance K833321 for LABOR/DELIVERY/RECOVERY BED LDR-600, Substantially Equivalent on 1983-11-14. Applicant: Adel Medical , Ltd.. Device class: 2.

Clearance details

Applicant: Adel Medical , Ltd.
Product code: Code KNC
Device class: Class 2
Regulation: 21 CFR 884.4900
Advisory panel: Obstetrics/Gynecology
Date received: 1983-09-26
Decision date: 1983-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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