Esophageal Dilator Set

FDA 510(k) K842679 · Mill-Rose Laboratory

Substantially Equivalent

510(k) numberK842679

Submission

Device name
Esophageal Dilator Set
Applicant
Mill-Rose Laboratory
Mchenry, IL, US
Received
July 10, 1984
Decision date
October 2, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FAT – Bougie, Esophageal, And Gastrointestinal, Gastro-Urology
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5365
Specialty
Gastroenterology, Urology

Other 510(k)s with product code FAT

510(k)DeviceApplicantDecision
K133439Pilling Esophageal BougiesFAT · Traditional Teleflexmedical, Inc.06/16/2014SE
K983220Stryker Infravision Esophageal KitFAT · Traditional Stryker Endoscopy06/04/1999SE
K972119Maloney Bouge (1210-XX)/HURST Bougie (1212-XX)FAT · Traditional Medovations, Inc.02/02/1998SE
K960173Infra Vision Bougie Kit, Infra Vision Esophageal KitFAT · Traditional Gabriel Medical, Inc.06/27/1996SE
K901425Pyloric Balloon DilatorFAT · Traditional Telemed Systems, Inc.06/21/1990SE
K843186Eska Multistage Esophageal BougieFAT · Traditional Dacomed Corp.01/18/1985SE
K780471Gastric Lavage KitFAT · Traditional Gaymar Industries, Inc.06/02/1978SE

More from Gaymar Industries, Inc.

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K971275Mill-Rose Disposable Polypectomy SnareFDI · Traditional 05/23/1997SE
K962736Mill-Rose Laryngoscopic Injection NeedleEOQ · Traditional 07/29/1996SE
K960880Mill-Rose Blind Microbiology BrushEOQ · Traditional 04/29/1996SE
K954519Wang Transendoscopic Aspiration NeedleFBK · Traditional 12/22/1995SE
K951600Mill-Rose Rotatable Polypectomy SnareFDI · Traditional 12/18/1995SE
K954745Mill-Rose Rigid Scope Cleaning BrushesFEB · Traditional 11/27/1995SE
K951051Rite-Bite Biopsy ForcepsEOQ · Traditional 03/24/1995SE
K951048Rite-Bite Biopsy ForcepsFCL · Traditional 03/15/1995SE

Questions and answers

When was Esophageal Dilator Set cleared by the FDA?

Esophageal Dilator Set (K842679) received a 510(k) decision of Substantially Equivalent on October 2, 1984, 84 days after the submission was received.

What is the product code of K842679?

The FDA product code is FAT – Bougie, Esophageal, And Gastrointestinal, Gastro-Urology, a Class II (moderate risk) device regulated under 21 CFR 876.5365.