Currettes, Alveolar (Molt and Miller)

FDA 510(k) K872091 · Military Engineering, Inc.

Substantially Equivalent

510(k) numberK872091

Submission

Device name
Currettes, Alveolar (Molt and Miller)
Applicant
Military Engineering, Inc.
Plymouth, IN, US
Received
June 1, 1987
Decision date
July 31, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EMS – Curette, Periodontic
Device class
Class I (low risk)
Regulation
21 CFR 872.4565
Specialty
Dental

Other 510(k)s with product code EMS

510(k)DeviceApplicantDecision
K931329Dental Instruments Curette PeriodontalEMS · Traditional Minnesota Prophy Power, Inc.01/27/1994SE
K870590Curette, Periodontal, Columbia UniversityEMS · Traditional Military Engineering, Inc.04/16/1987SE
K841011Elevator - VariousEMS · Traditional Premier Dental Products Co.06/15/1984SE
K834072Instrument, DentalEMS · Traditional Venture Technology, Inc.02/21/1984SE
K823319Dental Instruments - ScalersEMS · Traditional Miltex, Inc.11/24/1982SE
K821789Beach Curette No. 2 and No. 3 T.G.EMS · Traditional Pacific Dental Corp.07/06/1982SE

More from Pacific Dental Corp.

510(k)DeviceDecision
K874335Explorer-Dental ProberEKJ · Traditional 12/29/1987SE
K873715Bone Pin Cutter 18HXZ · Traditional 10/28/1987SE
K872842Pin, Hip, KnowlesHTY · Traditional 08/07/1987SE
K871834Drill, Hand, Bone, SmedbergDZJ · Traditional 07/31/1987SE
K872738Cortical Bone ScrewsHWC · Traditional 07/30/1987SE
K872609Curette Set, Antrum, CoakleyKAP · Traditional 07/15/1987SE
K871818Spatula, Dental, CementEJB · Traditional 07/02/1987SE
K872092Osteotome Set, Hoke, Straight, Set of 5KDG · Traditional 06/23/1987SE
K870590Curette, Periodontal, Columbia UniversityEMS · Traditional 04/16/1987SE
K871195Mallet, Bone Surgery, Stainless Steel, 2LB.HXL · Traditional 04/06/1987SE

Questions and answers

When was Currettes, Alveolar (Molt and Miller) cleared by the FDA?

Currettes, Alveolar (Molt and Miller) (K872091) received a 510(k) decision of Substantially Equivalent on July 31, 1987, 60 days after the submission was received.

What is the product code of K872091?

The FDA product code is EMS – Curette, Periodontic, a Class I (low risk) device regulated under 21 CFR 872.4565.