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FDA 510(k)

EXPLORER-DENTAL PROBER

K-Number: K874335 · 1987-12-29

Decision Date1987-12-29
Product CodeEKJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EXPLORER-DENTAL PROBER is the device name listed in this FDA 510(k) record. The listed applicant is Military Engineering, Inc.. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K874335. The device is classified under product code EKJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXPLORER-DENTAL PROBER?

EXPLORER-DENTAL PROBER is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Military Engineering, Inc.. The 510(k) number is K874335.

When did EXPLORER-DENTAL PROBER receive FDA 510(k) clearance?

EXPLORER-DENTAL PROBER received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874335.

Who is the listed applicant for EXPLORER-DENTAL PROBER?

The FDA 510(k) record lists Military Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXPLORER-DENTAL PROBER?

The FDA product code for EXPLORER-DENTAL PROBER is EKJ.

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 Military Engineering, Inc. 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: EKJ)

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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