VITAL PAK— 510(k) K955417

Unknown

Vital Signs, Inc.

FDA 510(k) clearance K955417 for VITAL PAK, Unknown on 1996-03-08. Applicant: Vital Signs, Inc.. Device class: 2.

Clearance details

Applicant: Vital Signs, Inc.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1995-11-27
Decision date: 1996-03-08
Decision: Unknown
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.