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FDA 510(k)

DLMS-ZIRBLOCKS

K-Number: K082137 · 2009-02-10

Decision Date2009-02-10
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DLMS-ZIRBLOCKS is the device name listed in this FDA 510(k) record. The listed applicant is Dental Milling Laboratory Supplies (Dlms). It received FDA 510(k) clearance on 2009-02-10 under 510(k) number K082137. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DLMS-ZIRBLOCKS?

DLMS-ZIRBLOCKS is a medical device that received FDA 510(k) clearance on 2009-02-10. The listed applicant is Dental Milling Laboratory Supplies (Dlms). The 510(k) number is K082137.

When did DLMS-ZIRBLOCKS receive FDA 510(k) clearance?

DLMS-ZIRBLOCKS received FDA 510(k) clearance on 2009-02-10, under 510(k) number K082137.

Who is the listed applicant for DLMS-ZIRBLOCKS?

The FDA 510(k) record lists Dental Milling Laboratory Supplies (Dlms) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DLMS-ZIRBLOCKS?

The FDA product code for DLMS-ZIRBLOCKS is EIH.

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.

Related Devices (Code: EIH)

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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