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FDA 510(k)

NO. 100352 GALVANIC OXYGEN SENSOR

K-Number: K862113 · 1986-06-19

ApplicantVascular Technology Incorporated
Decision Date1986-06-19
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NO. 100352 GALVANIC OXYGEN SENSOR 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 1986-06-19 under 510(k) number K862113. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NO. 100352 GALVANIC OXYGEN SENSOR?

NO. 100352 GALVANIC OXYGEN SENSOR is a medical device that received FDA 510(k) clearance on 1986-06-19. The listed applicant is Vascular Technology Incorporated. The 510(k) number is K862113.

When did NO. 100352 GALVANIC OXYGEN SENSOR receive FDA 510(k) clearance?

NO. 100352 GALVANIC OXYGEN SENSOR received FDA 510(k) clearance on 1986-06-19, under 510(k) number K862113.

Who is the listed applicant for NO. 100352 GALVANIC OXYGEN SENSOR?

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 NO. 100352 GALVANIC OXYGEN SENSOR?

The FDA product code for NO. 100352 GALVANIC OXYGEN SENSOR is CCL.

Related Clinical Trials

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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.

K082870VTI INTRAOPERATIVE DOPPLER SYSTEMSK031091VTI 20 MHZ GATED DOPPLERK002990VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001K944764VTI DISPOSABLE PRESSURE DISPLAY SETK922738VTI OXYGEN ANALYZERK890058VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM

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Related Devices (Code: CCL)

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.

K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter LabsK251245OxyMinder Pro (10310)Bio-Med Device, Inc.K250002Smart Check O2 (MA0236)Life Spark Medical, LLCK221734Maxtec MaxO2 ME+pMaxtec, LLCK213933Percent Oxygen SensorsCareox, LLCK213948OxyMinderBio-Med Devices, Inc.

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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