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FDA 510(k)

ASC-12 PIEZOELECTRIC SCALER

K-Number: K070866 · 2007-04-11

ApplicantAseptico, Inc.
Decision Date2007-04-11
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ASC-12 PIEZOELECTRIC SCALER is the device name listed in this FDA 510(k) record. The listed applicant is Aseptico, Inc.. It received FDA 510(k) clearance on 2007-04-11 under 510(k) number K070866. 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 ASC-12 PIEZOELECTRIC SCALER?

ASC-12 PIEZOELECTRIC SCALER is a medical device that received FDA 510(k) clearance on 2007-04-11. The listed applicant is Aseptico, Inc.. The 510(k) number is K070866.

When did ASC-12 PIEZOELECTRIC SCALER receive FDA 510(k) clearance?

ASC-12 PIEZOELECTRIC SCALER received FDA 510(k) clearance on 2007-04-11, under 510(k) number K070866.

Who is the listed applicant for ASC-12 PIEZOELECTRIC SCALER?

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

What is the FDA product code for ASC-12 PIEZOELECTRIC SCALER?

The FDA product code for ASC-12 PIEZOELECTRIC SCALER is ELC.

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Related Devices (Code: 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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