Tubing Handpiece Replacement

FDA 510(k) K854697 · Almore Intl., Inc.

Substantially Equivalent

510(k) numberK854697

Submission

Device name
Tubing Handpiece Replacement
Applicant
Almore Intl., Inc.
Portland, OR, US
Received
November 21, 1985
Decision date
March 6, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EFB – Handpiece, Air-Powered, Dental
Device class
Class I (low risk)
Regulation
21 CFR 872.4200
Specialty
Dental

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More from Ttbio Corp.

510(k)DeviceDecision
K862851Almore Face Mask · Traditional 08/12/1986SE
K854692Monarch II Bleaching InstrumentEEG · Traditional 05/12/1986SE
K854696Op II Visible Light Curing SystemEBZ · Traditional 03/26/1986SE
K854691Diamond Burs-HandpieceEJL · Traditional 03/25/1986SE
K854690Diamonds Burs-Composit FinishingEJL · Traditional 03/25/1986SE
K854700Ez-On Tubing Conditioner (Lubricant) · Traditional 03/12/1986SE
K854702Plastic Mounting RingsEJP · Traditional 03/06/1986SE
K854701Retract-A-CordJES · Traditional 03/06/1986SE
K854699Tubing SyringECB · Traditional 01/06/1986SE
K831136Double Bow Tooth SeparatorJEP · Traditional 06/08/1983SE

Questions and answers

When was Tubing Handpiece Replacement cleared by the FDA?

Tubing Handpiece Replacement (K854697) received a 510(k) decision of Substantially Equivalent on March 6, 1986, 105 days after the submission was received.

What is the product code of K854697?

The FDA product code is EFB – Handpiece, Air-Powered, Dental, a Class I (low risk) device regulated under 21 CFR 872.4200.