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FDA 510(k)

TIGER 500 SERIES HIGH SPEED HANDPIECES AND ATTACHMENTS

K-Number: K102517 · 2011-04-27

Decision Date2011-04-27
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TIGER 500 SERIES HIGH SPEED HANDPIECES AND ATTACHMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Thunder Tiger Corp.. It received FDA 510(k) clearance on 2011-04-27 under 510(k) number K102517. 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 TIGER 500 SERIES HIGH SPEED HANDPIECES AND ATTACHMENTS?

TIGER 500 SERIES HIGH SPEED HANDPIECES AND ATTACHMENTS is a medical device that received FDA 510(k) clearance on 2011-04-27. The listed applicant is Thunder Tiger Corp.. The 510(k) number is K102517.

When did TIGER 500 SERIES HIGH SPEED HANDPIECES AND ATTACHMENTS receive FDA 510(k) clearance?

TIGER 500 SERIES HIGH SPEED HANDPIECES AND ATTACHMENTS received FDA 510(k) clearance on 2011-04-27, under 510(k) number K102517.

Who is the listed applicant for TIGER 500 SERIES HIGH SPEED HANDPIECES AND ATTACHMENTS?

The FDA 510(k) record lists Thunder Tiger Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TIGER 500 SERIES HIGH SPEED HANDPIECES AND ATTACHMENTS?

The FDA product code for TIGER 500 SERIES HIGH SPEED HANDPIECES AND ATTACHMENTS 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 Thunder Tiger Corp. 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.

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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