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FDA 510(k)

SIROAIR L AIR SCALER

K-Number: K033812 · 2004-02-23

Decision Date2004-02-23
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SIROAIR L AIR SCALER is the device name listed in this FDA 510(k) record. The listed applicant is Sirona Dental Systems GmbH. It received FDA 510(k) clearance on 2004-02-23 under 510(k) number K033812. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIROAIR L AIR SCALER?

SIROAIR L AIR SCALER is a medical device that received FDA 510(k) clearance on 2004-02-23. The listed applicant is Sirona Dental Systems GmbH. The 510(k) number is K033812.

When did SIROAIR L AIR SCALER receive FDA 510(k) clearance?

SIROAIR L AIR SCALER received FDA 510(k) clearance on 2004-02-23, under 510(k) number K033812.

Who is the listed applicant for SIROAIR L AIR SCALER?

The FDA 510(k) record lists Sirona Dental Systems GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIROAIR L AIR SCALER?

The FDA product code for SIROAIR L AIR SCALER is EFB.

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 Sirona Dental Systems GmbH 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 37 devices →

Related Devices (Code: EFB)

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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