NK RANGE OF MOTION SENSOR, MODEL RM002— 510(k) K914061

Name: FDA 510(k) clearance K914061
Creator: U.S. Food and Drug Administration
Published: 1991-12-09

Substantially Equivalent

Nk Biotechnical Engineering Co.

FDA 510(k) clearance K914061 for NK RANGE OF MOTION SENSOR, MODEL RM002, Substantially Equivalent on 1991-12-09. Applicant: Nk Biotechnical Engineering Co.. Device class: 1.

Clearance details

Applicant: Nk Biotechnical Engineering Co.
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1991-09-10
Decision date: 1991-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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