Micro Surgical Handle

FDA 510(k) K831996 · Visitec Co.

Substantially Equivalent

510(k) numberK831996

Submission

Device name
Micro Surgical Handle
Applicant
Visitec Co.
Mchenry, IL, US
Received
June 21, 1983
Decision date
July 12, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KYG – Device, Irrigation, Ocular Surgery
Device class
Class I (low risk)
Regulation
21 CFR 886.4360
Specialty
Ophthalmic

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More from Boston Surgical Products, Inc.

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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 Micro Surgical Handle cleared by the FDA?

Micro Surgical Handle (K831996) received a 510(k) decision of Substantially Equivalent on July 12, 1983, 21 days after the submission was received.

What is the product code of K831996?

The FDA product code is KYG – Device, Irrigation, Ocular Surgery, a Class I (low risk) device regulated under 21 CFR 886.4360.