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

MICROSTAAR INDIGO INJECTOR FOAM TIP SYSTEM

K Number: K073586 · Decision Mar 13, 2008
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
62
Applicant Total
22
Review Days
84

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Basic Information

Device Name
MICROSTAAR INDIGO INJECTOR FOAM TIP SYSTEM
K Number
K073586
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4300
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Staar Surgical Co.
Date Received
December 20, 2007
Decision Date
March 13, 2008
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.

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Other Clearances by Staar Surgical Co.

K Number Device Name
K090161 EPIPHANY INJECTION SYSTEM
K073591 MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM
K032412 RE-USEABLE MICROSTAAR INJECTOR, MSI-S
K020734 SURGE-FREE ASPIRATION ADAPTER
K983129 DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1)
K980696 FOAM TIP INJECTOR
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. →