BIOSELF 101— 510(k) K823209

Substantially Equivalent

Bioself, Inc.

FDA 510(k) clearance K823209 for BIOSELF 101, Substantially Equivalent on 1983-02-15. Applicant: Bioself, Inc.. Device class: Unclassified.

Clearance details

Applicant: Bioself, Inc.
Product code: Code LHD
Device class: Unclassified
Advisory panel: Unknown
Date received: 1982-10-28
Decision date: 1983-02-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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