STRYKER LEG EXERCISER— 510(k) K831910

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K831910 for STRYKER LEG EXERCISER, Substantially Equivalent on 1983-07-12. Applicant: Stryker Corp.. Device class: 1.

Clearance details

Applicant: Stryker Corp.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1983-06-14
Decision date: 1983-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.