E550 ELECTROCARDIOGRAPH
K-Number: K883440 · 1989-01-17
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Device Summary
Frequently Asked Questions
What is the E550 ELECTROCARDIOGRAPH?
E550 ELECTROCARDIOGRAPH is a medical device that received FDA 510(k) clearance on 1989-01-17. The listed applicant is Burdick Corp.. The 510(k) number is K883440.
When did E550 ELECTROCARDIOGRAPH receive FDA 510(k) clearance?
E550 ELECTROCARDIOGRAPH received FDA 510(k) clearance on 1989-01-17, under 510(k) number K883440.
Who is the listed applicant for E550 ELECTROCARDIOGRAPH?
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 E550 ELECTROCARDIOGRAPH?
The FDA product code for E550 ELECTROCARDIOGRAPH is DSI.
Related Clinical Trials
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.
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.
Related Devices (Code: DSI)
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.
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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