ORTHO-J, INC. BEK-JS-004— 510(k) K891917

Substantially Equivalent

Ortho-J, Inc.

FDA 510(k) clearance K891917 for ORTHO-J, INC. BEK-JS-004, Substantially Equivalent on 1989-05-26. Applicant: Ortho-J, Inc.. Device class: 1.

Clearance details

Applicant: Ortho-J, Inc.
Product code: Code JEB
Device class: Class 1
Regulation: 21 CFR 878.4950
Advisory panel: General, Plastic Surgery
Date received: 1989-03-27
Decision date: 1989-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tifton, GA, US

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