MEDITRODE KIT— 510(k) K882554

Unknown

Life-Tech Intl., Inc.

FDA 510(k) clearance K882554 for MEDITRODE KIT, Unknown on 1988-12-23. Applicant: Life-Tech Intl., Inc.. Device class: 2.

Clearance details

Applicant: Life-Tech Intl., Inc.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 1988-06-21
Decision date: 1988-12-23
Decision: Unknown
Clearance type: Traditional
Location: Houston, TX, 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.