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

SPECTRALIS HRA+OCT, SPECTRALIS FA_OCT, SPECTRALIS ICGA+ OCT, SPECTRALIS HRA, SPECTRALIS FA

K Number: K101223 · Decision Oct 1, 2010
Classifications
1
FEI Numbers
29
Registration Numbers
30
Same Product Code
65
Applicant Total
9
Review Days
151

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Basic Information

Device Name
SPECTRALIS HRA+OCT, SPECTRALIS FA_OCT, SPECTRALIS ICGA+ OCT, SPECTRALIS HRA, SPECTRALIS FA
K Number
K101223
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heidelberg Engineering
Date Received
May 3, 2010
Decision Date
October 1, 2010
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

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Other Clearances by Heidelberg Engineering

K Number Device Name
K063191 HEIDELBERG RETINA ANGIOGRAPH 2/OPTICAL COHERENCE TOMOGRAPH, MODEL HRA 2/OCT
K052935 HEIDELBERG ENGINEERING SLITLAMP-OCT (SL-OCT)
K042742 HEIDELBERG RETINA TOMOGRAPH II / ROSTOCK CORNEA MODULE (HRT II / RCM)
K971671 HEIDELBERG RETINA ANGIOGRAPH FA/ICGA (HRA/C)
K943956 RETINA TOMOGRAPH AND FLOWMETER
K943955 RETINA FLOWMETER
K944261 RETINA ANGIOGRAPH
K912891 HEIDELBERG RETINA TOMOGRAPH