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Innolitics
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Review Panel
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Miscellaneous
Subpart B—Cardiovascular Diagnostic Devices
CFR Sub-Part
MOF
Guide, Wire, Catheter, Neurovasculature
2
Product Code
NDQ
System, Catheter Or Guidewire, Steerable (Magnetic)
2
Product Code
NRY
Catheter, Thrombus Retriever
2
Product Code
NUI
Ultrasound, Infusion, System
2
Product Code
QBE
Cranial Sound Monitor
2
Product Code
QJP
Catheter, Percutaneous, Neurovasculature
2
Product Code
K
24
0746
Neurovascular Access System Family
2
Cleared 510(K)
K
24
0711
Zipline Access Catheter
2
Cleared 510(K)
K
24
1244
CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter
2
Cleared 510(K)
K
24
0529
8F Modified Sheath System
2
Cleared 510(K)
K
23
4074
Next Generation Access Catheter
2
Cleared 510(K)
K
24
0948
TracStar LDP Large Distal Platform; Zoom 88 Large Distal Platform; Zoom 88 Large Distal Platform Support
2
Cleared 510(K)
K
23
2542
Wedge XL Delivery Catheter
2
Cleared 510(K)
K
23
3982
CEREGLIDE 92 Catheter System
2
Cleared 510(K)
K
23
3924
EMBOGUARD Balloon Guide Catheter
2
Cleared 510(K)
K
23
3201
MIDWAY Delivery Catheter (MIDWAY 43 Delivery Catheter; MIDWAY 62 Delivery Catheter)
2
Cleared 510(K)
Show All 61 Submissions
Subpart B—Diagnostic Devices
CFR Sub-Part
Subpart B—Neurological Diagnostic Devices
CFR Sub-Part
Subpart B—Physical Medicine Diagnostic Devices
CFR Sub-Part
Subpart C—Cardiovascular Monitoring Devices
CFR Sub-Part
Subpart D—Physical Medicine Prosthetic Devices
CFR Sub-Part
Subpart E—Neurological Surgical Devices
CFR Sub-Part
Subpart E—Surgical Devices
CFR Sub-Part
Subpart F—Cardiovascular 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
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 6 December 2024 at 11:05 pm
NE
/
subpart-b—cardiovascular-diagnostic-devices
/
QJP
/
K233982
View Source
CEREGLIDE 92 Catheter System
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233982
510(k) Type
Special
Applicant
Cerenovus Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2024
Days to Decision
143 days
Submission Type
Summary
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Miscellaneous
Subpart B—Cardiovascular Diagnostic Devices
MOF
Guide, Wire, Catheter, Neurovasculature
NDQ
System, Catheter Or Guidewire, Steerable (Magnetic)
NRY
Catheter, Thrombus Retriever
NUI
Ultrasound, Infusion, System
QBE
Cranial Sound Monitor
QJP
Catheter, Percutaneous, Neurovasculature
K
24
0746
Neurovascular Access System Family
K
24
0711
Zipline Access Catheter
K
24
1244
CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter
K
24
0529
8F Modified Sheath System
K
23
4074
Next Generation Access Catheter
K
24
0948
TracStar LDP Large Distal Platform; Zoom 88 Large Distal Platform; Zoom 88 Large Distal Platform Support
K
23
2542
Wedge XL Delivery Catheter
K
23
3982
CEREGLIDE 92 Catheter System
K
23
3924
EMBOGUARD Balloon Guide Catheter
K
23
3201
MIDWAY Delivery Catheter (MIDWAY 43 Delivery Catheter; MIDWAY 62 Delivery Catheter)
Show All 61 Submissions
Subpart B—Diagnostic Devices
Subpart B—Neurological Diagnostic Devices
Subpart B—Physical Medicine Diagnostic Devices
Subpart C—Cardiovascular Monitoring Devices
Subpart D—Physical Medicine Prosthetic Devices
Subpart E—Neurological Surgical Devices
Subpart E—Surgical Devices
Subpart F—Cardiovascular Therapeutic Devices
Subpart F—Neurological Therapeutic Devices
Subpart F—Physical Medicine Therapeutic Devices
Subpart F—Therapeutic Devices
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
NE
/
subpart-b—cardiovascular-diagnostic-devices
/
QJP
/
K233982
View Source
CEREGLIDE 92 Catheter System
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233982
510(k) Type
Special
Applicant
Cerenovus Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2024
Days to Decision
143 days
Submission Type
Summary