LIDO TM ACTIVE BACK— 510(k) K884487

Substantially Equivalent

Loredan Biomedical, Inc.

FDA 510(k) clearance K884487 for LIDO TM ACTIVE BACK, Substantially Equivalent on 1988-11-18. Applicant: Loredan Biomedical, Inc..

Clearance details

Applicant: Loredan Biomedical, Inc.
Product code: Code IKK
Advisory panel: Physical Medicine
Date received: 1988-10-25
Decision date: 1988-11-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Davis, CA, US

Download summary PDF View on FDA.gov ↗

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