FDA 510(k)

DACA-100

K-Number: K882933 · 1989-02-08

Decision Date1989-02-08

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DACA-100 is the device name listed in this FDA 510(k) record. The listed applicant is Visual Cybernetics. It received FDA 510(k) clearance on 1989-02-08 under 510(k) number K882933. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DACA-100?

DACA-100 is a medical device that received FDA 510(k) clearance on 1989-02-08. The listed applicant is Visual Cybernetics. The 510(k) number is K882933.

When did DACA-100 receive FDA 510(k) clearance?

DACA-100 received FDA 510(k) clearance on 1989-02-08, under 510(k) number K882933.

Who is the listed applicant for DACA-100?

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

What is the FDA product code for DACA-100?

The FDA product code for DACA-100 is LLZ.

Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.