CODA MPX30 MOTION ANALYSIS SYSTEM
K-Number: K982425 · 1998-10-07
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Device Summary
Frequently Asked Questions
What is the CODA MPX30 MOTION ANALYSIS SYSTEM?
CODA MPX30 MOTION ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1998-10-07. The listed applicant is Pinsco Inc. Dba B & L Engineering. The 510(k) number is K982425.
When did CODA MPX30 MOTION ANALYSIS SYSTEM receive FDA 510(k) clearance?
CODA MPX30 MOTION ANALYSIS SYSTEM received FDA 510(k) clearance on 1998-10-07, under 510(k) number K982425.
Who is the listed applicant for CODA MPX30 MOTION ANALYSIS SYSTEM?
The FDA 510(k) record lists Pinsco Inc. Dba B & L Engineering as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CODA MPX30 MOTION ANALYSIS SYSTEM?
The FDA product code for CODA MPX30 MOTION ANALYSIS SYSTEM is LXJ.
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 Pinsco Inc. Dba B & L Engineering 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: LXJ)
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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