Needles, Cannulas, Cystotomes

FDA 510(k) K782169 · Visitec Co.

Substantially Equivalent

510(k) numberK782169

Submission

Device name
Needles, Cannulas, Cystotomes
Applicant
Visitec Co.
Walker, MI, US
Received
December 29, 1978
Decision date
February 13, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HMX – Cannula, Ophthalmic
Device class
Class I (low risk)
Regulation
21 CFR 886.4350
Specialty
Ophthalmic

Other 510(k)s with product code HMX

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K010305Weiss Retinal CannulaHMX · Traditional Micron Surgical, Inc.05/02/2001SE
K000457Vertefusion-Photodynamic Therapy Pak, Model 11000 Series; Photofusion-Photodynamic…HMX · Traditional Retinalabs.Com05/09/2000SE
K970873Endosoft Soft Tip Needle (20 Ga. and 19 Ga.)HMX · Traditional American Medical Devices, Inc.05/20/1997SE
K943932Steriseal Ophthalmic CannulaHMX · Traditional Pharma-Plast, Ltd.01/18/1995SE
K942403Infusion CannulaHMX · Traditional Microsurgical Technology, Inc.08/17/1994SE
K934844Inter Tip THMX · Traditional Microsurgical Technology, Inc.04/19/1994SE
K930113Kirwan Irrigation/Aspiration HandpieceHMX · Traditional Kirwan Surgical Products, Inc.02/17/1994SE
K921488Aspirating Endo Ocular Probe W/IlluminationHMX · Traditional Surgical Technologies, Inc.05/07/1992SE
K915074Irrigator/Aspirator ProbeHMX · Traditional Biomedical Dynamics, Inc.02/05/1992SE
K904074Vitreoretinal Infusion CannulaHMX · Traditional Visitec Co.02/26/1991SE

More from Visitec Co.

510(k)DeviceDecision
K953394Visitec Collar Button Catheter {Griffiths}LZU · Traditional 10/12/1995SE
K945114Visitec Scleral PlugLXP · Traditional 02/23/1995SE
K945738Visiflex Ophthalmic Surgical Incise DrapeHMT · Traditional 02/14/1995SE
K945172Visitec Silicone Retinal Implants/ExplantsHQX · Traditional 01/17/1995SE
K942234Visitec Precise-PointGAP · Traditional 07/12/1994SE
K934269Fiberoptic Illuminated InstrumentsHJM · Traditional 05/17/1994SE
K940210Visitec Eye PadEFQ · Traditional 03/07/1994SE
K933872Visi-Spear Eye SpongeHOZ · Traditional 12/27/1993SE
K923972Ophthalmic Fluid Distribution SetsFPK · Traditional 11/04/1992SE
K922530Visitec Microsurgical SutureGAR · Traditional 10/20/1992SE

Questions and answers

When was Needles, Cannulas, Cystotomes cleared by the FDA?

Needles, Cannulas, Cystotomes (K782169) received a 510(k) decision of Substantially Equivalent on February 13, 1979, 46 days after the submission was received.

What is the product code of K782169?

The FDA product code is HMX – Cannula, Ophthalmic, a Class I (low risk) device regulated under 21 CFR 886.4350.