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FDA 510(k)

PATHWAY - ATS/CHEPS

K-Number: K052357 · 2006-01-19

Decision Date2006-01-19
Product CodeNTU
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PATHWAY - ATS/CHEPS is the device name listed in this FDA 510(k) record. The listed applicant is Medoc Ltd. Advanced Medical Systems. It received FDA 510(k) clearance on 2006-01-19 under 510(k) number K052357. The device is classified under product code NTU. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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