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FDA 510(k)

BP TRANSDUCER HOLDERS TH-2,3 & 4

K-Number: K832384 · 1983-11-14

Decision Date1983-11-14
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BP TRANSDUCER HOLDERS TH-2,3 & 4 is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1983-11-14 under 510(k) number K832384. The device is classified under product code DXO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BP TRANSDUCER HOLDERS TH-2,3 & 4?

BP TRANSDUCER HOLDERS TH-2,3 & 4 is a medical device that received FDA 510(k) clearance on 1983-11-14. The listed applicant is American Bentley. The 510(k) number is K832384.

When did BP TRANSDUCER HOLDERS TH-2,3 & 4 receive FDA 510(k) clearance?

BP TRANSDUCER HOLDERS TH-2,3 & 4 received FDA 510(k) clearance on 1983-11-14, under 510(k) number K832384.

Who is the listed applicant for BP TRANSDUCER HOLDERS TH-2,3 & 4?

The FDA 510(k) record lists American Bentley as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BP TRANSDUCER HOLDERS TH-2,3 & 4?

The FDA product code for BP TRANSDUCER HOLDERS TH-2,3 & 4 is DXO.

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 American Bentley 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.

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Related Devices (Code: DXO)

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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