PSI FLEXIBLE ARM
K-Number: K942601 · 1994-12-27
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Device Summary
Frequently Asked Questions
What is the PSI FLEXIBLE ARM?
PSI FLEXIBLE ARM is a medical device that received FDA 510(k) clearance on 1994-12-27. The listed applicant is V. Mueller Neuro/Spine. The 510(k) number is K942601.
When did PSI FLEXIBLE ARM receive FDA 510(k) clearance?
PSI FLEXIBLE ARM received FDA 510(k) clearance on 1994-12-27, under 510(k) number K942601.
Who is the listed applicant for PSI FLEXIBLE ARM?
The FDA 510(k) record lists V. Mueller Neuro/Spine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PSI FLEXIBLE ARM?
The FDA product code for PSI FLEXIBLE ARM is GCJ.
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 V. Mueller Neuro/Spine 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: GCJ)
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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