THE TUCKER SLING— 510(k) K932636

Substantially Equivalent

Tucker Designs, Ltd.

FDA 510(k) clearance K932636 for THE TUCKER SLING, Substantially Equivalent on 1994-01-26. Applicant: Tucker Designs, Ltd.. Device class: 1.

Clearance details

Applicant: Tucker Designs, Ltd.
Product code: Code FRP
Device class: Class 1
Regulation: 21 CFR 880.5680
Advisory panel: General Hospital
Date received: 1993-06-02
Decision date: 1994-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kenner, LA, US

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