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FDA 510(k)

CARDIOFAX ECG-6353

K-Number: K860212 · 1986-04-17

ApplicantNihon Kohden America, Inc.
Decision Date1986-04-17
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIOFAX ECG-6353 is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden America, Inc.. It received FDA 510(k) clearance on 1986-04-17 under 510(k) number K860212. 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 CARDIOFAX ECG-6353?

CARDIOFAX ECG-6353 is a medical device that received FDA 510(k) clearance on 1986-04-17. The listed applicant is Nihon Kohden America, Inc.. The 510(k) number is K860212.

When did CARDIOFAX ECG-6353 receive FDA 510(k) clearance?

CARDIOFAX ECG-6353 received FDA 510(k) clearance on 1986-04-17, under 510(k) number K860212.

Who is the listed applicant for CARDIOFAX ECG-6353?

The FDA 510(k) record lists Nihon Kohden America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARDIOFAX ECG-6353?

The FDA product code for CARDIOFAX ECG-6353 is DPS.

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Other records listing Nihon Kohden America, 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.

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Related Devices (Code: DPS)

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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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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