INTERCEPT— 510(k) K843591

Substantially Equivalent

Vital Signs, Inc.

FDA 510(k) clearance K843591 for INTERCEPT, Substantially Equivalent on 1984-10-19. Applicant: Vital Signs, Inc.. Device class: 2.

Clearance details

Applicant: Vital Signs, Inc.
Product code: Code KDP
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1984-09-12
Decision date: 1984-10-19
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.