Goggle Safeguard

FDA 510(k) K944857 · Sellstrom Mfg. Co.

Substantially Equivalent

510(k) numberK944857

Submission

Device name
Goggle Safeguard
Applicant
Sellstrom Mfg. Co.
Palatine, IL, US
Received
September 30, 1994
Decision date
December 15, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
HOY – Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
Device class
Class I (low risk)
Regulation
21 CFR 886.4750
Specialty
Ophthalmic

Other 510(k)s with product code HOY

510(k)DeviceApplicantDecision
K132042AMB101 System, Amblyz, LCG System, XpandHOY · Traditional X6d, Ltd.04/28/2014SE
K050856LCG (Liquide Crystal Glasses) SystemHOY · Traditional Ophthocare , Ltd.05/31/2005SE
K971465National Medical Halthcare Custom Ophthalmic Kits or TraysHOY · Traditional National Healthcare Mfg. Corp.06/04/1997SE
K944700Arctic Premier SeriesHOY · Traditional Sungold Eyewear, Inc.12/22/1994SE
K945351Shield, Eye, OphthalmicHOY · Traditional Taiwan Eva Industrial Co., Inc.12/13/1994SE
K945346Makrolon 2405 Goggles (Light and Dark)HOY · Traditional Universal Massage & Tanning, Inc.11/22/1994SE
K942407Amcon Slip in Mydriatic SunglassesHOY · Traditional Amcon Laboratories, Inc.06/06/1994SE
K941829Sun Filters/ShieldsHOY · Traditional Klinger Eye Shields, Inc.05/17/1994SE
K930347Shaids Protective GlassesHOY · Traditional Depuy, Inc.04/29/1994SE
K940275Universal Cushioned Polycarbonat Eye ShieldHOY · Traditional P.J. Products, Inc.03/24/1994SE

More from P.J. Products, Inc.

510(k)DeviceDecision
K931254Goggle SafeguardHOY · Traditional 11/12/1993SE

Questions and answers

When was Goggle Safeguard cleared by the FDA?

Goggle Safeguard (K944857) received a 510(k) decision of Substantially Equivalent on December 15, 1994, 76 days after the submission was received.

What is the product code of K944857?

The FDA product code is HOY – Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear), a Class I (low risk) device regulated under 21 CFR 886.4750.