Disposable Microstaar Injector (Model MSI-P1)

FDA 510(k) K983129 · Staar Surgical Co.

Substantially Equivalent

510(k) numberK983129

Submission

Device name
Disposable Microstaar Injector (Model MSI-P1)
Applicant
Staar Surgical Co.
Monrovia, CA, US
Received
September 8, 1998
Decision date
December 4, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KYB – Lens, Guide, Intraocular
Device class
Class I (low risk)
Regulation
21 CFR 886.4300
Specialty
Ophthalmic

Other 510(k)s with product code KYB

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K152357MicroSTAAR Injector System CartridgesKYB · Special STAAR Surgical Company10/30/2015SE
K081382Duckworth & Kent, Ltd., Implantation System, Model DK7786KYB · Traditional Duckworth & Kent, Ltd.10/23/2008SE
K072985Duckworth & Kent Ltd Injector, Model: DK7797-2KYB · Traditional Duckworth & Kent, Ltd.06/20/2008SE
K070669Iol Injector SetKYB · Traditional Medicel AG11/01/2007SE
K063155Monarch III Iol Delivery SystemKYB · Traditional Alcon Manufacturing, Ltd.03/27/2007SE
K063694Akreos Single Use Insertion Device, Model AI-28KYB · Special Bausch & Lomb, Inc.03/07/2007SE
K032412Re-Useable Microstaar Injector, Msi-SKYB · Traditional Staar Surgical Co.06/10/2004SE
K022723Mastel 1 Folder Implantation SystemKYB · Traditional Mastel Precision, Inc.12/26/2002SE
K001157Monarch II Iol Delivery SystemKYB · Traditional Alcon Research, Ltd.06/27/2000SE
K981571Monarch Iol Delivery SystemKYB · Traditional Alcon Laboratories07/09/1998SE

More from Alcon Laboratories

510(k)DeviceDecision
K172375MicroSTAAR Injector System CartridgesMSS · Special 09/06/2017SE
K152357MicroSTAAR Injector System CartridgesKYB · Special 10/30/2015SE
K090161Epiphany Injection SystemMSS · Traditional 06/09/2009SE
K073591Microstaar Msi Injector Foam Tip SystemMSS · Traditional 03/13/2008SE
K073586Microstaar Indigo Injector Foam Tip SystemMSS · Traditional 03/13/2008SE
K032412Re-Useable Microstaar Injector, Msi-SKYB · Traditional 06/10/2004SE
K020734Surge-Free Aspiration AdapterHQC · Traditional 05/16/2002SE
K980696Foam Tip InjectorMSS · Traditional 09/11/1998SE
K954600Microstaar Injector Models Msi-Td & Msi-Pd (Modification)KYB · Traditional 12/21/1995SE
K913626Softrans InjectorHQL · Traditional 12/18/1991SE

Questions and answers

When was Disposable Microstaar Injector (Model MSI-P1) cleared by the FDA?

Disposable Microstaar Injector (Model MSI-P1) (K983129) received a 510(k) decision of Substantially Equivalent on December 4, 1998, 87 days after the submission was received.

What is the product code of K983129?

The FDA product code is KYB – Lens, Guide, Intraocular, a Class I (low risk) device regulated under 21 CFR 886.4300.