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FDA 510(k)

DYE MANAGEMENT SYSTEM

K-Number: K933700 · 1993-11-03

ApplicantAbbott Laboratories
Decision Date1993-11-03
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DYE MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1993-11-03 under 510(k) number K933700. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYE MANAGEMENT SYSTEM?

DYE MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1993-11-03. The listed applicant is Abbott Laboratories. The 510(k) number is K933700.

When did DYE MANAGEMENT SYSTEM receive FDA 510(k) clearance?

DYE MANAGEMENT SYSTEM received FDA 510(k) clearance on 1993-11-03, under 510(k) number K933700.

Who is the listed applicant for DYE MANAGEMENT SYSTEM?

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

What is the FDA product code for DYE MANAGEMENT SYSTEM?

The FDA product code for DYE MANAGEMENT SYSTEM is DQO.

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Related Devices (Code: DQO)

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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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