FDA 510(k)

PROPHYLAXIS ANGLE

K-Number: K790722 · 1979-06-15

ApplicantYoung Dental Manufacturing Co. 1, LLC

Decision Date1979-06-15

Product CodeEGS

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

PROPHYLAXIS ANGLE is the device name listed in this FDA 510(k) record. The listed applicant is Young Dental Manufacturing Co. 1, LLC. It received FDA 510(k) clearance on 1979-06-15 under 510(k) number K790722. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROPHYLAXIS ANGLE?

PROPHYLAXIS ANGLE is a medical device that received FDA 510(k) clearance on 1979-06-15. The listed applicant is Young Dental Manufacturing Co. 1, LLC. The 510(k) number is K790722.

When did PROPHYLAXIS ANGLE receive FDA 510(k) clearance?

PROPHYLAXIS ANGLE received FDA 510(k) clearance on 1979-06-15, under 510(k) number K790722.

Who is the listed applicant for PROPHYLAXIS ANGLE?

The FDA 510(k) record lists Young Dental Manufacturing Co. 1, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROPHYLAXIS ANGLE?

The FDA product code for PROPHYLAXIS ANGLE is EGS.

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Other records listing Young Dental Manufacturing Co. 1, LLC as applicant

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Related Devices (Code: EGS)

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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.