THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK— 510(k) K925225

Name: FDA 510(k) clearance K925225
Creator: U.S. Food and Drug Administration
Published: 1994-06-27

Substantially Equivalent

Baltimore Therapeutic Equipment Co.

FDA 510(k) clearance K925225 for THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK, Substantially Equivalent on 1994-06-27. Applicant: Baltimore Therapeutic Equipment Co.. Device class: 1.

Clearance details

Applicant: Baltimore Therapeutic Equipment Co.
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1992-10-16
Decision date: 1994-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hanover, MD, 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.