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FDA 510(k)

MK 700 ULTRASOUND SYSTEM

K-Number: K842093 · 1984-09-27

ApplicantAdvanced Technology Laboratories, Inc.
Decision Date1984-09-27
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MK 700 ULTRASOUND SYSTEM 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 1984-09-27 under 510(k) number K842093. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MK 700 ULTRASOUND SYSTEM?

MK 700 ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 1984-09-27. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K842093.

When did MK 700 ULTRASOUND SYSTEM receive FDA 510(k) clearance?

MK 700 ULTRASOUND SYSTEM received FDA 510(k) clearance on 1984-09-27, under 510(k) number K842093.

Who is the listed applicant for MK 700 ULTRASOUND SYSTEM?

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 MK 700 ULTRASOUND SYSTEM?

The FDA product code for MK 700 ULTRASOUND SYSTEM is IYO.

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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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