RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM— 510(k) K941781

Name: FDA 510(k) clearance K941781
Creator: U.S. Food and Drug Administration
Published: 1994-08-25

Substantially Equivalent

Dacomed Corp.

FDA 510(k) clearance K941781 for RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM, Substantially Equivalent on 1994-08-25. Applicant: Dacomed Corp.. Device class: Unclassified.

Clearance details

Applicant: Dacomed Corp.
Product code: Code LIL
Device class: Unclassified
Advisory panel: Unknown
Date received: 1994-04-11
Decision date: 1994-08-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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