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FDA 510(k)

TITANE SL DENTAL BURR

K-Number: K872471 · 1987-09-11

ApplicantTitane SL Co.
Decision Date1987-09-11
Product CodeECM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TITANE SL DENTAL BURR is the device name listed in this FDA 510(k) record. The listed applicant is Titane SL Co.. It received FDA 510(k) clearance on 1987-09-11 under 510(k) number K872471. The device is classified under product code ECM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITANE SL DENTAL BURR?

TITANE SL DENTAL BURR is a medical device that received FDA 510(k) clearance on 1987-09-11. The listed applicant is Titane SL Co.. The 510(k) number is K872471.

When did TITANE SL DENTAL BURR receive FDA 510(k) clearance?

TITANE SL DENTAL BURR received FDA 510(k) clearance on 1987-09-11, under 510(k) number K872471.

Who is the listed applicant for TITANE SL DENTAL BURR?

The FDA 510(k) record lists Titane SL Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TITANE SL DENTAL BURR?

The FDA product code for TITANE SL DENTAL BURR is ECM.

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.

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Related Devices (Code: ECM)

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.

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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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