RSVP SYSTEMS, SERIES I, BED-PATIENT MONITOR— 510(k) K864827

Name: FDA 510(k) clearance K864827
Creator: U.S. Food and Drug Administration
Published: 1987-01-21

Substantially Equivalent

Tactilitics, Inc.

FDA 510(k) clearance K864827 for RSVP SYSTEMS, SERIES I, BED-PATIENT MONITOR, Substantially Equivalent on 1987-01-21. Applicant: Tactilitics, Inc.. Device class: 1.

Clearance details

Applicant: Tactilitics, Inc.
Product code: Code KMI
Device class: Class 1
Regulation: 21 CFR 880.2400
Advisory panel: General Hospital
Date received: 1986-12-09
Decision date: 1987-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boulder, CO, US

Download summary PDF View on FDA.gov ↗

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