Nalgene Emergency Eye Wash

FDA 510(k) K760820 · Nagle Co.

Substantially Equivalent

510(k) numberK760820

Submission

Device name
Nalgene Emergency Eye Wash
Applicant
Nagle Co.
Mchenry, IL, US
Received
October 13, 1976
Decision date
October 20, 1976
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

Other 510(k)s with product code KYG

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K993591Bladeworks Disposable Alk TubingKYG · Traditional Blade Works, Inc.12/28/1999SE
K981116Sovereign Cataract Extraction SystemKYG · Traditional Allergan, Inc.05/19/1998SE
K980647Eye Irrigator Model #2020KYG · Traditional Eye-Deal Ocular Safety Products, Inc.05/15/1998SE
K974561Moistair Fluid Air Tubing SetKYG · Traditional American Medical Devices, Inc.02/19/1998SE
K971173ML Disposable Alk TubingKYG · Traditional Med-Logics, Inc.05/22/1997SE
K970161Hedges Corneal Wetting PakKYG · Traditional Hedges Cwp, Inc.03/25/1997SE
K954842D.O.R.C. Vfi/Vfe SystemKYG · Traditional Dutch Ophthalmic USA, Inc.04/15/1996SE
K945171Disposable & Resuable Irrigation/Aspiration HandpieceKYG · Traditional Boston Surgical Products, Inc.02/08/1995SE

Questions and answers

When was Nalgene Emergency Eye Wash cleared by the FDA?

Nalgene Emergency Eye Wash (K760820) received a 510(k) decision of Substantially Equivalent on October 20, 1976, 7 days after the submission was received.

What is the product code of K760820?

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