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FDA 510(k)

BP-TEL TRANS-TELEPHONIC BLOOD PRESSURE MEASUREMENT SYSTEM

K-Number: K983717 · 1999-09-16

Decision Date1999-09-16
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BP-TEL TRANS-TELEPHONIC BLOOD PRESSURE MEASUREMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aerotel Medical Systems (1998) , Ltd.. It received FDA 510(k) clearance on 1999-09-16 under 510(k) number K983717. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BP-TEL TRANS-TELEPHONIC BLOOD PRESSURE MEASUREMENT SYSTEM?

BP-TEL TRANS-TELEPHONIC BLOOD PRESSURE MEASUREMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1999-09-16. The listed applicant is Aerotel Medical Systems (1998) , Ltd.. The 510(k) number is K983717.

When did BP-TEL TRANS-TELEPHONIC BLOOD PRESSURE MEASUREMENT SYSTEM receive FDA 510(k) clearance?

BP-TEL TRANS-TELEPHONIC BLOOD PRESSURE MEASUREMENT SYSTEM received FDA 510(k) clearance on 1999-09-16, under 510(k) number K983717.

Who is the listed applicant for BP-TEL TRANS-TELEPHONIC BLOOD PRESSURE MEASUREMENT SYSTEM?

The FDA 510(k) record lists Aerotel Medical Systems (1998) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BP-TEL TRANS-TELEPHONIC BLOOD PRESSURE MEASUREMENT SYSTEM?

The FDA product code for BP-TEL TRANS-TELEPHONIC BLOOD PRESSURE MEASUREMENT SYSTEM is DXN.

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 Medical Systems (1998) , 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.

View all 7 devices →

Related Devices (Code: DXN)

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

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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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