NK GRASP SENSOR, MODEL GA001— 510(k) K923964

Name: FDA 510(k) clearance K923964
Creator: U.S. Food and Drug Administration
Published: 1993-05-12

Substantially Equivalent

Nk Biotechnical Engineering Co.

FDA 510(k) clearance K923964 for NK GRASP SENSOR, MODEL GA001, Substantially Equivalent on 1993-05-12. Applicant: Nk Biotechnical Engineering Co.. Device class: 2.

Clearance details

Applicant: Nk Biotechnical Engineering Co.
Product code: Code LBB
Device class: Class 2
Regulation: 21 CFR 888.1240
Advisory panel: Orthopedic
Date received: 1992-08-07
Decision date: 1993-05-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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