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FDA 510(k)

MARK 500 SYSTEM

K-Number: K810073 · 1981-03-05

ApplicantAdvanced Technology Laboratories, Inc.
Decision Date1981-03-05
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MARK 500 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 1981-03-05 under 510(k) number K810073. 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 MARK 500 SYSTEM?

MARK 500 SYSTEM is a medical device that received FDA 510(k) clearance on 1981-03-05. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K810073.

When did MARK 500 SYSTEM receive FDA 510(k) clearance?

MARK 500 SYSTEM received FDA 510(k) clearance on 1981-03-05, under 510(k) number K810073.

Who is the listed applicant for MARK 500 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 MARK 500 SYSTEM?

The FDA product code for MARK 500 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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