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FDA 510(k)

NTE-2 THERMAL SENSITIVITY TESTER

K-Number: K864345 · 1987-01-29

ApplicantSensortek, Inc.
Decision Date1987-01-29
Product CodeLQW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NTE-2 THERMAL SENSITIVITY TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Sensortek, Inc.. It received FDA 510(k) clearance on 1987-01-29 under 510(k) number K864345. The device is classified under product code LQW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NTE-2 THERMAL SENSITIVITY TESTER?

NTE-2 THERMAL SENSITIVITY TESTER is a medical device that received FDA 510(k) clearance on 1987-01-29. The listed applicant is Sensortek, Inc.. The 510(k) number is K864345.

When did NTE-2 THERMAL SENSITIVITY TESTER receive FDA 510(k) clearance?

NTE-2 THERMAL SENSITIVITY TESTER received FDA 510(k) clearance on 1987-01-29, under 510(k) number K864345.

Who is the listed applicant for NTE-2 THERMAL SENSITIVITY TESTER?

The FDA 510(k) record lists Sensortek, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NTE-2 THERMAL SENSITIVITY TESTER?

The FDA product code for NTE-2 THERMAL SENSITIVITY TESTER is LQW.

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.

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Other records listing Sensortek, Inc. 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.

K863607VIBRATRON II, VIBRATION SENSITIVITY TESTERK852228ESOPHAGEAL STETHOSCOPE WITH ELECTRICAL CONDUCTORSK844056THERMOCOUPLE SENSORS, ACCESS. FOR ELECTRONIC THERMK844055ESOPHAGEAL STETHO SCOPE

Related Devices (Code: LQW)

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.

K922052TSA 2001 THERMAL SENSORY ANALYZERMedoc Corp.

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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