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FDA 510(k)

ULTRASOUND 72X & ANNULAR ARRAY SCAN-

K-Number: K843165 · 1984-12-20

ApplicantAdvanced Technology Laboratories, Inc.
Decision Date1984-12-20
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ULTRASOUND 72X & ANNULAR ARRAY SCAN- is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Technology Laboratories, Inc.. It received FDA 510(k) clearance on 1984-12-20 under 510(k) number K843165. 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 ULTRASOUND 72X & ANNULAR ARRAY SCAN-?

ULTRASOUND 72X & ANNULAR ARRAY SCAN- is a medical device that received FDA 510(k) clearance on 1984-12-20. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K843165.

When did ULTRASOUND 72X & ANNULAR ARRAY SCAN- receive FDA 510(k) clearance?

ULTRASOUND 72X & ANNULAR ARRAY SCAN- received FDA 510(k) clearance on 1984-12-20, under 510(k) number K843165.

Who is the listed applicant for ULTRASOUND 72X & ANNULAR ARRAY SCAN-?

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

What is the FDA product code for ULTRASOUND 72X & ANNULAR ARRAY SCAN-?

The FDA product code for ULTRASOUND 72X & ANNULAR ARRAY SCAN- is JOP.

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Related Devices (Code: JOP)

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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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