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FDA 510(k)

MULTICHANNEL TELEMETRY SYSTEM

K-Number: K801944 · 1980-10-23

ApplicantBurdick Corp.
Decision Date1980-10-23
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULTICHANNEL TELEMETRY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Burdick Corp.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K801944. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTICHANNEL TELEMETRY SYSTEM?

MULTICHANNEL TELEMETRY SYSTEM is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Burdick Corp.. The 510(k) number is K801944.

When did MULTICHANNEL TELEMETRY SYSTEM receive FDA 510(k) clearance?

MULTICHANNEL TELEMETRY SYSTEM received FDA 510(k) clearance on 1980-10-23, under 510(k) number K801944.

Who is the listed applicant for MULTICHANNEL TELEMETRY SYSTEM?

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 MULTICHANNEL TELEMETRY SYSTEM?

The FDA product code for MULTICHANNEL TELEMETRY SYSTEM is DRG.

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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: DRG)

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.

K261569UbiqVue™ 2AYe Cardiac System (UX2253)Lifesignals, Inc.K252984Perin Health System (PHD80060-2)Perin Health Devices, LLCK252440EasyTeleMed (2.0.2)Ingeniars S.R.L.K250259TeleRehab Aermos Cardiopulmonary RehabilitationThe ScottCare CorporationK243837iBSMIorbit Digital Technologies Private LimitedK242018UbiqVue™ 2A Multi-parameter System (UX2550)Lifesignals, 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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