RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM
K-Number: K941781 · 1994-08-25
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Device Summary
Frequently Asked Questions
What is the RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM?
RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1994-08-25. The listed applicant is Dacomed Corp.. The 510(k) number is K941781.
When did RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM receive FDA 510(k) clearance?
RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM received FDA 510(k) clearance on 1994-08-25, under 510(k) number K941781.
Who is the listed applicant for RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM?
The FDA 510(k) record lists Dacomed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM?
The FDA product code for RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM is LIL.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Dacomed Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LIL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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