KENDRICK EXTRICATION DEVICE— 510(k) K781761

Substantially Equivalent

Medi-Ked, Inc.

FDA 510(k) clearance K781761 for KENDRICK EXTRICATION DEVICE, Substantially Equivalent on 1978-10-27. Applicant: Medi-Ked, Inc.. Device class: 1.

Clearance details

Applicant: Medi-Ked, Inc.
Product code: Code IQF
Device class: Class 1
Regulation: 21 CFR 890.3490
Advisory panel: Physical Medicine
Date received: 1978-10-16
Decision date: 1978-10-27
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.