Jetpolisher(Tm)

FDA 510(k) K875340 · Young Dental Manufacturing Co. 1, LLC

Substantially Equivalent

510(k) numberK875340

Submission

Device name
Jetpolisher(Tm)
Applicant
Young Dental Manufacturing Co. 1, LLC
Earth City, MO, US
Received
December 30, 1987
Decision date
June 10, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KOJ – Airbrush
Device class
Class II (moderate risk)
Regulation
21 CFR 872.6080
Specialty
Dental

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More from Deldent , Ltd.

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K932255Young D'GranulatorKMW · Traditional 04/15/1994SE
K903284Young Prophy System, PS UnitKOJ · Traditional 12/17/1990SE
K875339Jetpolisher Airpolishing PowderEJR · Traditional 04/18/1988SE
K821484Dawn Low Speed Handpiece SystemEFB · Traditional 06/09/1982SE
K790723Prophylaxis Cups and PolishersEHK · Traditional 06/15/1979SE
K790722Prophylaxis AngleEGS · Traditional 06/15/1979SE

Questions and answers

When was Jetpolisher(Tm) cleared by the FDA?

Jetpolisher(Tm) (K875340) received a 510(k) decision of Substantially Equivalent on June 10, 1988, 163 days after the submission was received.

What is the product code of K875340?

The FDA product code is KOJ – Airbrush, a Class II (moderate risk) device regulated under 21 CFR 872.6080.