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FDA 510(k)

M300 MONITOR/CONTROLLER T500 TREADMILL

K-Number: K873774 · 1987-11-06

ApplicantBurdick Corp.
Decision Date1987-11-06
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

M300 MONITOR/CONTROLLER T500 TREADMILL is the device name listed in this FDA 510(k) record. The listed applicant is Burdick Corp.. It received FDA 510(k) clearance on 1987-11-06 under 510(k) number K873774. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M300 MONITOR/CONTROLLER T500 TREADMILL?

M300 MONITOR/CONTROLLER T500 TREADMILL is a medical device that received FDA 510(k) clearance on 1987-11-06. The listed applicant is Burdick Corp.. The 510(k) number is K873774.

When did M300 MONITOR/CONTROLLER T500 TREADMILL receive FDA 510(k) clearance?

M300 MONITOR/CONTROLLER T500 TREADMILL received FDA 510(k) clearance on 1987-11-06, under 510(k) number K873774.

Who is the listed applicant for M300 MONITOR/CONTROLLER T500 TREADMILL?

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

What is the FDA product code for M300 MONITOR/CONTROLLER T500 TREADMILL?

The FDA product code for M300 MONITOR/CONTROLLER T500 TREADMILL is DXJ.

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Other records listing Burdick Corp. 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.

K942565ALTAIR-DISC RECORDERK941351BURDICK PRO2 OXIMETERK904032ELITE II ELECTROCARDIOGRAPHK903565E560 ELECTROCARDIOGRAPHK900729NEOSERV 824K885085ERGOMED 840/ERGOMED 840L

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Related Devices (Code: DXJ)

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.

K212003ESSENZ Patient MonitorLivanova Deutschland, GmbHK212208Philips IntelliVue GuardianSoftware (Rev. E.0X)Philips Medizin Systeme Boeblingen GmbHK201162Essence 55SP Large Monitor SystemShenyang Torch-Bigtide Digital Technology Co., Ltd.K173107Vios Central Station Monitor Software, Vios Central Server SoftwareVios Medical, Inc.K180534Philips IntelliVue GuardianSoftwarePhilips Medizin Systeme Boeblingen GmbHK173381Nexxis ORBarco N.V.

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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