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FDA 510(k)

IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT

K-Number: K894151 · 1989-09-27

ApplicantArtech Corp.
Decision Date1989-09-27
Product CodeDZJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT is the device name listed in this FDA 510(k) record. The listed applicant is Artech Corp.. It received FDA 510(k) clearance on 1989-09-27 under 510(k) number K894151. The device is classified under product code DZJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT?

IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT is a medical device that received FDA 510(k) clearance on 1989-09-27. The listed applicant is Artech Corp.. The 510(k) number is K894151.

When did IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT receive FDA 510(k) clearance?

IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT received FDA 510(k) clearance on 1989-09-27, under 510(k) number K894151.

Who is the listed applicant for IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT?

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

What is the FDA product code for IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT?

The FDA product code for IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT is DZJ.

Related Clinical Trials

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.

Other records listing Artech Corp. as applicant

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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Related Devices (Code: DZJ)

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.

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.

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