Digital Electrocardiograph
K-Number: K171517 · 2018-01-11
Device Summary
Frequently Asked Questions
What is the Digital Electrocardiograph?
Digital Electrocardiograph is a medical device that received FDA 510(k) clearance on 2018-01-11. The listed applicant is Biocare Bio-Medical Equipment Co., Ltd.. The 510(k) number is K171517.
When did Digital Electrocardiograph receive FDA 510(k) clearance?
Digital Electrocardiograph received FDA 510(k) clearance on 2018-01-11, under 510(k) number K171517.
Who is the listed applicant for Digital Electrocardiograph?
The FDA 510(k) record lists Biocare Bio-Medical Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Digital Electrocardiograph?
The FDA product code for Digital Electrocardiograph is DPS.
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.
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.