HEARTLINE TRANSTELEPHONIC ECG RECEIVING CONSOLE
K-Number: K930314 · 1994-03-18
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Device Summary
Frequently Asked Questions
What is the HEARTLINE TRANSTELEPHONIC ECG RECEIVING CONSOLE?
HEARTLINE TRANSTELEPHONIC ECG RECEIVING CONSOLE is a medical device that received FDA 510(k) clearance on 1994-03-18. The listed applicant is Aerotel, Ltd.. The 510(k) number is K930314.
When did HEARTLINE TRANSTELEPHONIC ECG RECEIVING CONSOLE receive FDA 510(k) clearance?
HEARTLINE TRANSTELEPHONIC ECG RECEIVING CONSOLE received FDA 510(k) clearance on 1994-03-18, under 510(k) number K930314.
Who is the listed applicant for HEARTLINE TRANSTELEPHONIC ECG RECEIVING CONSOLE?
The FDA 510(k) record lists Aerotel, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEARTLINE TRANSTELEPHONIC ECG RECEIVING CONSOLE?
The FDA product code for HEARTLINE TRANSTELEPHONIC ECG RECEIVING CONSOLE is DXH. This falls under the Hematology category.
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 Aerotel, Ltd. 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: DXH)
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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