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FDA 510(k)

EPX-310 VIDEO PROCESSOR (ENDOSCOPY)

K-Number: K950417 · 1995-07-21

Decision Date1995-07-21
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EPX-310 VIDEO PROCESSOR (ENDOSCOPY) is the device name listed in this FDA 510(k) record. The listed applicant is Marks & Murase. It received FDA 510(k) clearance on 1995-07-21 under 510(k) number K950417. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPX-310 VIDEO PROCESSOR (ENDOSCOPY)?

EPX-310 VIDEO PROCESSOR (ENDOSCOPY) is a medical device that received FDA 510(k) clearance on 1995-07-21. The listed applicant is Marks & Murase. The 510(k) number is K950417.

When did EPX-310 VIDEO PROCESSOR (ENDOSCOPY) receive FDA 510(k) clearance?

EPX-310 VIDEO PROCESSOR (ENDOSCOPY) received FDA 510(k) clearance on 1995-07-21, under 510(k) number K950417.

Who is the listed applicant for EPX-310 VIDEO PROCESSOR (ENDOSCOPY)?

The FDA 510(k) record lists Marks & Murase as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPX-310 VIDEO PROCESSOR (ENDOSCOPY)?

The FDA product code for EPX-310 VIDEO PROCESSOR (ENDOSCOPY) is FET.

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 Marks & Murase 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: FET)

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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