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FDA 510(k)

LAVA FRAME, LAVA FRAME SHADE

K-Number: K072055 · 2008-02-26

Decision Date2008-02-26
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LAVA FRAME, LAVA FRAME SHADE is the device name listed in this FDA 510(k) record. The listed applicant is 3M Espe AG Dental Products. It received FDA 510(k) clearance on 2008-02-26 under 510(k) number K072055. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAVA FRAME, LAVA FRAME SHADE?

LAVA FRAME, LAVA FRAME SHADE is a medical device that received FDA 510(k) clearance on 2008-02-26. The listed applicant is 3M Espe AG Dental Products. The 510(k) number is K072055.

When did LAVA FRAME, LAVA FRAME SHADE receive FDA 510(k) clearance?

LAVA FRAME, LAVA FRAME SHADE received FDA 510(k) clearance on 2008-02-26, under 510(k) number K072055.

Who is the listed applicant for LAVA FRAME, LAVA FRAME SHADE?

The FDA 510(k) record lists 3M Espe AG Dental Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAVA FRAME, LAVA FRAME SHADE?

The FDA product code for LAVA FRAME, LAVA FRAME SHADE is NHA.

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 3M Espe AG Dental Products 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.

View all 24 devices →

Related Devices (Code: NHA)

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

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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