PATHWAY - ATS/CHEPS
K-Number: K052357 · 2006-01-19
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Device Summary
Frequently Asked Questions
What is the PATHWAY - ATS/CHEPS?
PATHWAY - ATS/CHEPS is a medical device that received FDA 510(k) clearance on 2006-01-19. The listed applicant is Medoc Ltd. Advanced Medical Systems. The 510(k) number is K052357.
When did PATHWAY - ATS/CHEPS receive FDA 510(k) clearance?
PATHWAY - ATS/CHEPS received FDA 510(k) clearance on 2006-01-19, under 510(k) number K052357.
Who is the listed applicant for PATHWAY - ATS/CHEPS?
The FDA 510(k) record lists Medoc Ltd. Advanced Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATHWAY - ATS/CHEPS?
The FDA product code for PATHWAY - ATS/CHEPS is NTU.
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 Medoc Ltd. Advanced Medical 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: NTU)
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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