Search Results
Found 1 results
510(k) Data Aggregation
K Number
K022723Device Name
MASTEL 1 FOLDER IMPLANTATION SYSTEM
Manufacturer
MASTEL PRECISION, INC.
Date Cleared
2002-12-26
(132 days)
Product Code
KYB
Regulation Number
886.4300Why did this record match?
Applicant Name (Manufacturer) :
MASTEL PRECISION, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Mastel 1 Folder™ Implantation System is intended to fold and assist in inserting the SENSAR™, model AR40e intraocular lens, ONLY into the capsular bag.
Device Description
The Mastel 1 Folder is an ophthalmic surgical device designed for use in inserting a foldable intraocular lens into the eye. The materials, basic scientific concepts, physical properties and intended use of the Mastel 1 Folder are similar to those of the predicate devices.
The Mastel 1 Folder Implantation System is comprised of a medical-grade titanium handpiece, a material commonly used in reusable surgical devices. The handpiece rod is designed to accept a single-use cartridge. The handpiece is reusable and is designed to withstand conventional in-office steam autoclaving. The handpiece is provided to the customer in a plastic case in a non-sterile state.
Ask a Question
Page 1 of 1