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FDA 510(k)

SCORPION ULTRASONIC SCALING INSERTS

K-Number: K053578 · 2006-07-14

ApplicantScorpion
Decision Date2006-07-14
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SCORPION ULTRASONIC SCALING INSERTS is the device name listed in this FDA 510(k) record. The listed applicant is Scorpion. It received FDA 510(k) clearance on 2006-07-14 under 510(k) number K053578. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCORPION ULTRASONIC SCALING INSERTS?

SCORPION ULTRASONIC SCALING INSERTS is a medical device that received FDA 510(k) clearance on 2006-07-14. The listed applicant is Scorpion. The 510(k) number is K053578.

When did SCORPION ULTRASONIC SCALING INSERTS receive FDA 510(k) clearance?

SCORPION ULTRASONIC SCALING INSERTS received FDA 510(k) clearance on 2006-07-14, under 510(k) number K053578.

Who is the listed applicant for SCORPION ULTRASONIC SCALING INSERTS?

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

What is the FDA product code for SCORPION ULTRASONIC SCALING INSERTS?

The FDA product code for SCORPION ULTRASONIC SCALING INSERTS is ELC.

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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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