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FDA 510(k)

STATIS DENTAL HANDPIECES

K-Number: K071891 · 2007-09-13

ApplicantScican , Ltd.
Decision Date2007-09-13
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STATIS DENTAL HANDPIECES is the device name listed in this FDA 510(k) record. The listed applicant is Scican , Ltd.. It received FDA 510(k) clearance on 2007-09-13 under 510(k) number K071891. 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 STATIS DENTAL HANDPIECES?

STATIS DENTAL HANDPIECES is a medical device that received FDA 510(k) clearance on 2007-09-13. The listed applicant is Scican , Ltd.. The 510(k) number is K071891.

When did STATIS DENTAL HANDPIECES receive FDA 510(k) clearance?

STATIS DENTAL HANDPIECES received FDA 510(k) clearance on 2007-09-13, under 510(k) number K071891.

Who is the listed applicant for STATIS DENTAL HANDPIECES?

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

What is the FDA product code for STATIS DENTAL HANDPIECES?

The FDA product code for STATIS DENTAL HANDPIECES 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 Scican , Ltd. 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 11 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

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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