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FDA 510(k)

ELECTROCARDIOGRAPH, EK-7 (3-CHANNELS)

K-Number: K760271 · 1976-11-15

ApplicantBurdick Corp.
Decision Date1976-11-15
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTROCARDIOGRAPH, EK-7 (3-CHANNELS) is the device name listed in this FDA 510(k) record. The listed applicant is Burdick Corp.. It received FDA 510(k) clearance on 1976-11-15 under 510(k) number K760271. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROCARDIOGRAPH, EK-7 (3-CHANNELS)?

ELECTROCARDIOGRAPH, EK-7 (3-CHANNELS) is a medical device that received FDA 510(k) clearance on 1976-11-15. The listed applicant is Burdick Corp.. The 510(k) number is K760271.

When did ELECTROCARDIOGRAPH, EK-7 (3-CHANNELS) receive FDA 510(k) clearance?

ELECTROCARDIOGRAPH, EK-7 (3-CHANNELS) received FDA 510(k) clearance on 1976-11-15, under 510(k) number K760271.

Who is the listed applicant for ELECTROCARDIOGRAPH, EK-7 (3-CHANNELS)?

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 ELECTROCARDIOGRAPH, EK-7 (3-CHANNELS)?

The FDA product code for ELECTROCARDIOGRAPH, EK-7 (3-CHANNELS) is DPS.

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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 OXIMETERK903565E560 ELECTROCARDIOGRAPHK904032ELITE II ELECTROCARDIOGRAPHK900729NEOSERV 824K885085ERGOMED 840/ERGOMED 840L

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Related Devices (Code: DPS)

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K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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