FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

P200TE (A10700)

K Number: K231673 · Decision Aug 18, 2023
Classifications
1
FEI Numbers
29
Registration Numbers
30
Same Product Code
65
Applicant Total
15
Review Days
71

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
P200TE (A10700)
K Number
K231673
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Optos Plc.
Date Received
June 8, 2023
Decision Date
August 18, 2023
Product Code
OBO
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
OBO Tomography, Optical Coherence

Similar 510(k) Clearances

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

View all

Other Clearances by Optos Plc.

K Number Device Name
K233602 P200TE (A10700)
K190732 P200TxE
K173707 P200TE
K162039 OptosAdvance 4.0 Software
K142897 P200DTx
K134039 DAYTONA ICG (P200TICG)
K121043 OPTOS OCT/SLO MICROPERIMETER
K113696 OPTOS ADVANCE
K111628 P200T
K102492 P200MAAF
Search all 15 clearances from Optos Plc. →