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FDA 510(k)

Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM

K-Number: K992874 · 1999-11-18

ApplicantWr Medical Electronics Co.
Decision Date1999-11-18
Product CodeKTB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wr Medical Electronics Co.. It received FDA 510(k) clearance on 1999-11-18 under 510(k) number K992874. The device is classified under product code KTB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM?

Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1999-11-18. The listed applicant is Wr Medical Electronics Co.. The 510(k) number is K992874.

When did Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM receive FDA 510(k) clearance?

Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM received FDA 510(k) clearance on 1999-11-18, under 510(k) number K992874.

Who is the listed applicant for Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM?

The FDA 510(k) record lists Wr Medical Electronics Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM?

The FDA product code for Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM is KTB.

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 Wr Medical Electronics Co. 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.

K092809HRV ACQUIREK063560HILGER DUAL-STIM NERVE STIMULATORK000574IONTOPHORETIC DRUG DELIVERY ELECTRODE, IONTOPHORETIC ELECTRODE (ACTIVE)K910624CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4K895838BRACKMANN EMG MONITORING SYSTEM

Related Devices (Code: KTB)

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.

K180627Macroduct Advanced Model 3710Elitechgroup, Inc.K033192RH-950Iomed, Inc.K031551NORTHSTAR LIDOCAINE IONTOPHORETIC CONTROLLER (NORTHSTAR CONTROLLER-D)Vyteris, Inc.K031115RH-900Iomed, Inc.K010031NANODUCT NEONATAL SWEAT ANALYSIS SYSTEMWescor, Inc.K001522TRANSQ3Iomed, 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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