FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

FOAM TIP INJECTOR

K Number: K980696 · Decision Sep 11, 1998
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
62
Applicant Total
22
Review Days
200

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
FOAM TIP INJECTOR
K Number
K980696
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4300
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Staar Surgical Co.
Date Received
February 23, 1998
Decision Date
September 11, 1998
Product Code
MSS
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MSS Folders And Injectors, Intraocular Lens (Iol)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MSS), ordered by most recent decision date.

View all

Other Clearances by Staar Surgical Co.

K Number Device Name
K090161 EPIPHANY INJECTION SYSTEM
K073591 MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM
K073586 MICROSTAAR INDIGO INJECTOR FOAM TIP SYSTEM
K032412 RE-USEABLE MICROSTAAR INJECTOR, MSI-S
K020734 SURGE-FREE ASPIRATION ADAPTER
K983129 DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1)
K954600 MICROSTAAR INJECTOR MODELS MSI-TD & MSI-PD (MODIFICATION)
K913626 SOFTRANS INJECTOR
K884241 STAAR PHACO XL SMALL INCISION SYSTEM
K875099 MOLTENO VALVE SETON
Search all 22 clearances from Staar Surgical Co. →