A-Dec/W&H Electric Motor, Model EA-50LT

FDA 510(k) K032572 · A-Dec, Inc.

Substantially Equivalent

510(k) numberK032572

Submission

Device name
A-Dec/W&H Electric Motor, Model EA-50LT
Applicant
A-Dec, Inc.
Newberg, OR, US
Received
August 20, 2003
Decision date
December 3, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
EBW – Controller, Foot, Handpiece And Cord
Device class
Class I (low risk)
Regulation
21 CFR 872.4200
Specialty
Dental

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More from Guilin Woodpecker Medical Instrument Co., Ltd.

510(k)DeviceDecision
K213932A-dec 300, A-dec 500EIA · Traditional 03/02/2022SE
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K102234A-Dec 200 Dental SystemEIA · Traditional 11/24/2010SE
K100647A-Dec/W&H Synea Sonic Scaler Handpiece, Models ZA-55, ZA-55 L, ZA-55 LM, ZA-55M, SF1LMELC · Traditional 07/09/2010SE
K082716A-Dec/W&H Alegra Air-Driven Highspeed Handpiece, Model TE-97, TE-98, A-Dec/W&H Alegra…EFB · Abbreviated 01/15/2009SE
K082827A-Dec/W&H Profin Reciprocating Contra-Angle Handpiece AttachmentEFB · Abbreviated 01/07/2009SE
K082985A-Dec 334/335 Delivery SystemEIA · Traditional 12/17/2008SE
K070663A-Dec/W&H Synea Air-Driven Highspeed Handpiece, Model TA-98, TA-97, A-Dec/W&H Synea…EFB · Abbreviated 07/05/2007SE
K051657A-Dec Self-Contained Water SystemEIA · Traditional 08/30/2005SE
K032757A-Dec Self-Contained Water System, Model 0.7 Liter Bottle & 2 Liter BottleEIA · Traditional 12/10/2003SE

Questions and answers

When was A-Dec/W&H Electric Motor, Model EA-50LT cleared by the FDA?

A-Dec/W&H Electric Motor, Model EA-50LT (K032572) received a 510(k) decision of Substantially Equivalent on December 3, 2003, 105 days after the submission was received.

What is the product code of K032572?

The FDA product code is EBW – Controller, Foot, Handpiece And Cord, a Class I (low risk) device regulated under 21 CFR 872.4200.