Cutter Jet

FDA 510(k) K801651 · Cutter Laboratories, Inc.

Substantially Equivalent

510(k) numberK801651

Submission

Device name
Cutter Jet
Applicant
Cutter Laboratories, Inc.
Mchenry, IL, US
Received
July 18, 1980
Decision date
August 13, 1980
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.

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K861315Hyperbaric Penetration Extension SetCBF · Traditional 05/21/1986SE
K854106BaysilexELW · Traditional 03/17/1986SE
K842324PerfourmELW · Traditional 11/09/1984SE
K834106Intravenous Infusion ControllerLDR · Traditional 05/30/1984SE
K832237Orthopedic Casting Tape MaxcastITG · Traditional 08/16/1983SE
K823214Dosimetric Release Program - Admin. SetFPA · Traditional 01/12/1983SE
K821326Cutter Bond Polycarboxylate CementEMA · Traditional 05/28/1982SE
K813532Cutterbond Zinc Phosphate CementEMA · Traditional 03/02/1982SE
K802105C-BladeHWE · Traditional 09/16/1980SE
K802104C-SplintIQI · Traditional 09/16/1980SE

Questions and answers

When was Cutter Jet cleared by the FDA?

Cutter Jet (K801651) received a 510(k) decision of Substantially Equivalent on August 13, 1980, 26 days after the submission was received.

What is the product code of K801651?

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