FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OPTOS ADVANCE

K Number: K113696 · Decision May 25, 2012
Classifications
1
FEI Numbers
31
Registration Numbers
32
Same Product Code
51
Applicant Total
15
Review Days
161

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
OPTOS ADVANCE
K Number
K113696
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Optos Plc.
Date Received
December 16, 2011
Decision Date
May 25, 2012
Product Code
NFJ
Advisory Committee
Radiology
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
NFJ System, Image Management, Ophthalmic

Similar 510(k) Clearances

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

View all

Other Clearances by Optos Plc.

K Number Device Name
K233602 P200TE (A10700)
K231673 P200TE (A10700)
K190732 P200TxE
K173707 P200TE
K162039 OptosAdvance 4.0 Software
K142897 P200DTx
K134039 DAYTONA ICG (P200TICG)
K121043 OPTOS OCT/SLO MICROPERIMETER
K111628 P200T
K102492 P200MAAF
Search all 15 clearances from Optos Plc. →