PAINDOC
K-Number: K021518 · 2002-06-06
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Device Summary
Frequently Asked Questions
What is the PAINDOC?
PAINDOC is a medical device that received FDA 510(k) clearance on 2002-06-06. The listed applicant is Advanced Neuromodulation Systems. The 510(k) number is K021518.
When did PAINDOC receive FDA 510(k) clearance?
PAINDOC received FDA 510(k) clearance on 2002-06-06, under 510(k) number K021518.
Who is the listed applicant for PAINDOC?
The FDA 510(k) record lists Advanced Neuromodulation Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PAINDOC?
The FDA product code for PAINDOC is GZB.
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 Advanced Neuromodulation Systems 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: GZB)
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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