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FDA 510(k)

TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT

K-Number: K891180 · 1989-06-15

ApplicantIngress Technologies, Inc.
Decision Date1989-06-15
Product CodeDXP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ingress Technologies, Inc.. It received FDA 510(k) clearance on 1989-06-15 under 510(k) number K891180. The device is classified under product code DXP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT?

TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT is a medical device that received FDA 510(k) clearance on 1989-06-15. The listed applicant is Ingress Technologies, Inc.. The 510(k) number is K891180.

When did TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT receive FDA 510(k) clearance?

TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT received FDA 510(k) clearance on 1989-06-15, under 510(k) number K891180.

Who is the listed applicant for TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT?

The FDA 510(k) record lists Ingress Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT?

The FDA product code for TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT is DXP.

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Related Devices (Code: DXP)

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

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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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