FLEX-ELBOW— 510(k) K912652

Substantially Equivalent

Vital Signs, Inc.

FDA 510(k) clearance K912652 for FLEX-ELBOW, Substantially Equivalent on 1991-10-10. Applicant: Vital Signs, Inc.. Device class: 1.

Clearance details

Applicant: Vital Signs, Inc.
Product code: Code BZA
Device class: Class 1
Regulation: 21 CFR 868.5810
Advisory panel: Anesthesiology
Date received: 1991-06-17
Decision date: 1991-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Totowa, NJ, 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.