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FDA 510(k)

TRANSESOPHAGEAL ECHOCARDIOGRAPHY ULTRASO

K-Number: K843262 · 1984-08-23

ApplicantHewlett-Packard Co.
Decision Date1984-08-23
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRANSESOPHAGEAL ECHOCARDIOGRAPHY ULTRASO is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1984-08-23 under 510(k) number K843262. The device is classified under product code JOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSESOPHAGEAL ECHOCARDIOGRAPHY ULTRASO?

TRANSESOPHAGEAL ECHOCARDIOGRAPHY ULTRASO is a medical device that received FDA 510(k) clearance on 1984-08-23. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K843262.

When did TRANSESOPHAGEAL ECHOCARDIOGRAPHY ULTRASO receive FDA 510(k) clearance?

TRANSESOPHAGEAL ECHOCARDIOGRAPHY ULTRASO received FDA 510(k) clearance on 1984-08-23, under 510(k) number K843262.

Who is the listed applicant for TRANSESOPHAGEAL ECHOCARDIOGRAPHY ULTRASO?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSESOPHAGEAL ECHOCARDIOGRAPHY ULTRASO?

The FDA product code for TRANSESOPHAGEAL ECHOCARDIOGRAPHY ULTRASO is JOP.

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Related Devices (Code: JOP)

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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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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