SINGLE USE NON-CONDUCTIVE CIRC. DISCON— 510(k) K821667

Name: FDA 510(k) clearance K821667
Creator: U.S. Food and Drug Administration
Published: 1982-06-24

Substantially Equivalent

Vital Signs, Inc.

FDA 510(k) clearance K821667 for SINGLE USE NON-CONDUCTIVE CIRC. DISCON, Substantially Equivalent on 1982-06-24. Applicant: Vital Signs, Inc.. Device class: 2.

Clearance details

Applicant: Vital Signs, Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1982-06-07
Decision date: 1982-06-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: East Rutherford, 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.