FDA Browser
by
Innolitics
Anesthesiology
Review Panel
Cardiovascular
Review Panel
Chemistry
Review Panel
Dental
Review Panel
Ear, Nose, Throat
Review Panel
Gastroenterology and Urology
Review Panel
General Hospital
Review Panel
Miscellaneous
Miscellaneous
Subpart B—Cardiovascular Diagnostic Devices
CFR Sub-Part
Subpart B—Diagnostic Devices
CFR Sub-Part
PUP
Endoscope Maintenance System
2
Product Code
FEB
Accessories, Cleaning, For Endoscope
2
Product Code
DEN
24
0018
CORIS System
2
Cleared 510(K)
K
24
1168
System 83 Revolve Endoscope Washer/Disinfector
2
Cleared 510(K)
K
24
3433
enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System
2
Cleared 510(K)
K
23
0930
enspire 3000 Cleaning and Liquid Chemical Sterile Processing System
2
Cleared 510(K)
K
21
3833
SCOPE BUDDY PLUS Endoscope Flushing Aid
2
Cleared 510(K)
K
20
1920
Endoscope Reprocessor OER-Elite
2
Cleared 510(K)
K
17
3590
System 83 Plus Washer/Disinfector
2
Cleared 510(K)
K
19
0969
ENDOSCOPE REPROCESSOR OER-Elite
2
Cleared 510(K)
K
18
1472
AEROFLEX(TM) Automatic Endoscope Reprocessor with AUTOSURE(TM) MRC Monitor
2
Cleared 510(K)
K
18
1865
Acu-sInQ Complete Endoscope Cleaning Aid System
2
Cleared 510(K)
Show All 58 Submissions
NVE
Washer, Cleaner, Automated, Endoscope
2
Product Code
NZA
Accessories, Germicide, Cleaning, For Endoscopes
2
Product Code
OUJ
High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Mist
2
Product Code
PSW
High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Liquid
2
Product Code
Subpart C—Cardiovascular Monitoring Devices
CFR Sub-Part
Subpart C—General Hospital and Personal Use Monitoring Devices
CFR Sub-Part
Subpart D—Pathology Instrumentation and Accessories
CFR Sub-Part
Subpart D—Prosthetic Devices
CFR Sub-Part
Subpart E—Surgical Devices
CFR Sub-Part
Subpart F—General Hospital and Personal Use Therapeutic Devices
CFR Sub-Part
Subpart F—Neurological Therapeutic Devices
CFR Sub-Part
Subpart F—Physical Medicine Therapeutic Devices
CFR Sub-Part
Subpart F—Therapeutic Devices
CFR Sub-Part
Subpart G—General Hospital and Personal Use Miscellaneous Devices
CFR Sub-Part
Subpart G—Miscellaneous Devices
CFR Sub-Part
Hematology
Review Panel
Immunology
Review Panel
Microbiology
Review Panel
Neurology
Review Panel
Obstetrical and Gynecological
Review Panel
Ophthalmic
Review Panel
Orthopedic
Review Panel
Pathology
Review Panel
Physical Medicine
Review Panel
Radiology
Review Panel
General and Plastic Surgery
Review Panel
Toxicology
Review Panel
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 2 May 2025 at 11:05 pm
HO
/
subpart-b—diagnostic-devices
/
FEB
/
K190969
View Source
ENDOSCOPE REPROCESSOR OER-Elite
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190969
510(k) Type
Traditional
Applicant
Olympus Medical Systems Corp.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/9/2019
Days to Decision
88 days
Submission Type
Summary
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Miscellaneous
Subpart B—Cardiovascular Diagnostic Devices
Subpart B—Diagnostic Devices
PUP
Endoscope Maintenance System
FEB
Accessories, Cleaning, For Endoscope
DEN
24
0018
CORIS System
K
24
1168
System 83 Revolve Endoscope Washer/Disinfector
K
24
3433
enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System
K
23
0930
enspire 3000 Cleaning and Liquid Chemical Sterile Processing System
K
21
3833
SCOPE BUDDY PLUS Endoscope Flushing Aid
K
20
1920
Endoscope Reprocessor OER-Elite
K
17
3590
System 83 Plus Washer/Disinfector
K
19
0969
ENDOSCOPE REPROCESSOR OER-Elite
K
18
1472
AEROFLEX(TM) Automatic Endoscope Reprocessor with AUTOSURE(TM) MRC Monitor
K
18
1865
Acu-sInQ Complete Endoscope Cleaning Aid System
Show All 58 Submissions
NVE
Washer, Cleaner, Automated, Endoscope
NZA
Accessories, Germicide, Cleaning, For Endoscopes
OUJ
High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Mist
PSW
High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Liquid
Subpart C—Cardiovascular Monitoring Devices
Subpart C—General Hospital and Personal Use Monitoring Devices
Subpart D—Pathology Instrumentation and Accessories
Subpart D—Prosthetic Devices
Subpart E—Surgical Devices
Subpart F—General Hospital and Personal Use Therapeutic Devices
Subpart F—Neurological Therapeutic Devices
Subpart F—Physical Medicine Therapeutic Devices
Subpart F—Therapeutic Devices
Subpart G—General Hospital and Personal Use Miscellaneous Devices
Subpart G—Miscellaneous Devices
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
HO
/
subpart-b—diagnostic-devices
/
FEB
/
K190969
View Source
ENDOSCOPE REPROCESSOR OER-Elite
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190969
510(k) Type
Traditional
Applicant
Olympus Medical Systems Corp.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/9/2019
Days to Decision
88 days
Submission Type
Summary