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FDA 510(k)

KHURI REGIONAL TISSUE PH MONITOR

K-Number: K862114 · 1986-06-25

Decision Date1986-06-25
Product CodeCBZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

KHURI REGIONAL TISSUE PH MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Technology Incorporated. It received FDA 510(k) clearance on 1986-06-25 under 510(k) number K862114. The device is classified under product code CBZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KHURI REGIONAL TISSUE PH MONITOR?

KHURI REGIONAL TISSUE PH MONITOR is a medical device that received FDA 510(k) clearance on 1986-06-25. The listed applicant is Vascular Technology Incorporated. The 510(k) number is K862114.

When did KHURI REGIONAL TISSUE PH MONITOR receive FDA 510(k) clearance?

KHURI REGIONAL TISSUE PH MONITOR received FDA 510(k) clearance on 1986-06-25, under 510(k) number K862114.

Who is the listed applicant for KHURI REGIONAL TISSUE PH MONITOR?

The FDA 510(k) record lists Vascular Technology Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KHURI REGIONAL TISSUE PH MONITOR?

The FDA product code for KHURI REGIONAL TISSUE PH MONITOR is CBZ.

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 Vascular Technology Incorporated 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.

View all 11 devices →

Related Devices (Code: CBZ)

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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