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FDA 510(k)

MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY

K-Number: K861710 · 1986-07-09

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1986-07-09
Product CodeDXK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1986-07-09 under 510(k) number K861710. The device is classified under product code DXK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY?

MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY is a medical device that received FDA 510(k) clearance on 1986-07-09. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K861710.

When did MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY receive FDA 510(k) clearance?

MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY received FDA 510(k) clearance on 1986-07-09, under 510(k) number K861710.

Who is the listed applicant for MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY?

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

What is the FDA product code for MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY?

The FDA product code for MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY is DXK.

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Related Devices (Code: DXK)

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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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