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FDA 510(k)

WASHINGTON CARDIAC MONITOR

K-Number: K903710 · 1990-11-09

ApplicantWashington Biolab, Inc.
Decision Date1990-11-09
Product CodeDXK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WASHINGTON CARDIAC MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Washington Biolab, Inc.. It received FDA 510(k) clearance on 1990-11-09 under 510(k) number K903710. The device is classified under product code DXK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WASHINGTON CARDIAC MONITOR?

WASHINGTON CARDIAC MONITOR is a medical device that received FDA 510(k) clearance on 1990-11-09. The listed applicant is Washington Biolab, Inc.. The 510(k) number is K903710.

When did WASHINGTON CARDIAC MONITOR receive FDA 510(k) clearance?

WASHINGTON CARDIAC MONITOR received FDA 510(k) clearance on 1990-11-09, under 510(k) number K903710.

Who is the listed applicant for WASHINGTON CARDIAC MONITOR?

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

What is the FDA product code for WASHINGTON CARDIAC MONITOR?

The FDA product code for WASHINGTON CARDIAC MONITOR is DXK.

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Related Devices (Code: DXK)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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