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FDA 510(k)

ARTUS DRILL #3000

K-Number: K803290 · 1981-01-28

ApplicantJedmed Instrument Co.
Decision Date1981-01-28
Product CodeDZI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ARTUS DRILL #3000 is the device name listed in this FDA 510(k) record. The listed applicant is Jedmed Instrument Co.. It received FDA 510(k) clearance on 1981-01-28 under 510(k) number K803290. The device is classified under product code DZI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTUS DRILL #3000?

ARTUS DRILL #3000 is a medical device that received FDA 510(k) clearance on 1981-01-28. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K803290.

When did ARTUS DRILL #3000 receive FDA 510(k) clearance?

ARTUS DRILL #3000 received FDA 510(k) clearance on 1981-01-28, under 510(k) number K803290.

Who is the listed applicant for ARTUS DRILL #3000?

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

What is the FDA product code for ARTUS DRILL #3000?

The FDA product code for ARTUS DRILL #3000 is DZI.

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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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