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FDA 510(k)

Forest Dental Unit

K-Number: K173608 · 2018-08-17

Decision Date2018-08-17
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Forest Dental Unit is the device name listed in this FDA 510(k) record. The listed applicant is Forest Dental Products, Inc.. It received FDA 510(k) clearance on 2018-08-17 under 510(k) number K173608. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Forest Dental Unit?

Forest Dental Unit is a medical device that received FDA 510(k) clearance on 2018-08-17. The listed applicant is Forest Dental Products, Inc.. The 510(k) number is K173608.

When did Forest Dental Unit receive FDA 510(k) clearance?

Forest Dental Unit received FDA 510(k) clearance on 2018-08-17, under 510(k) number K173608.

Who is the listed applicant for Forest Dental Unit?

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

What is the FDA product code for Forest Dental Unit?

The FDA product code for Forest Dental Unit is EIA.

Related Devices (Code: EIA)

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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