KNIGHTWATCH SYSTEM— 510(k) K896934

Substantially Equivalent

Createch Corp.

FDA 510(k) clearance K896934 for KNIGHTWATCH SYSTEM, Substantially Equivalent on 1990-06-25. Applicant: Createch Corp.. Device class: 2.

Clearance details

Applicant: Createch Corp.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1989-12-13
Decision date: 1990-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, D.C., DC, 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.