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FDA 510(k)

VIBRATRON II, VIBRATION SENSITIVITY TESTER

K-Number: K863607 · 1986-12-03

ApplicantSensortek, Inc.
Decision Date1986-12-03
Product CodeLLN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VIBRATRON II, VIBRATION 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 1986-12-03 under 510(k) number K863607. The device is classified under product code LLN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIBRATRON II, VIBRATION SENSITIVITY TESTER?

VIBRATRON II, VIBRATION SENSITIVITY TESTER is a medical device that received FDA 510(k) clearance on 1986-12-03. The listed applicant is Sensortek, Inc.. The 510(k) number is K863607.

When did VIBRATRON II, VIBRATION SENSITIVITY TESTER receive FDA 510(k) clearance?

VIBRATRON II, VIBRATION SENSITIVITY TESTER received FDA 510(k) clearance on 1986-12-03, under 510(k) number K863607.

Who is the listed applicant for VIBRATRON II, VIBRATION 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 VIBRATRON II, VIBRATION SENSITIVITY TESTER?

The FDA product code for VIBRATRON II, VIBRATION SENSITIVITY TESTER is LLN.

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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.

K864345NTE-2 THERMAL SENSITIVITY TESTERK852228ESOPHAGEAL STETHOSCOPE WITH ELECTRICAL CONDUCTORSK844056THERMOCOUPLE SENSORS, ACCESS. FOR ELECTRONIC THERMK844055ESOPHAGEAL STETHO SCOPE

Related Devices (Code: LLN)

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.

K072882PAIN VISION, MODEL PS-2100Osachi Co., Ltd.K030829VPT METERXilas Medical, Inc.K010981GSA GENITO SENSORY ANALYZERMedoc Ltd. Advanced Medical SystemsK964622MEDI-DX 7000Neuro-Diagnostic Assoc.K964815AP-4000, AIR PULSE SENSORY STIMULATORPentax Precision Instrument Corp.K970180VSA 3000 VIBRATORYN SENSORY ANALYZEREare Consulting Service

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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