FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

CavaClear Laser Sheath

K Number: DEN210024 · Decision Dec 21, 2021
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
0
Applicant Total
17
Review Days
179

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Basic Information

Device Name
CavaClear Laser Sheath
K Number
DEN210024
Device Class
FDA class 2
Clearance Type
Direct
Regulation Number
870.5125
Medical Specialty
Cardiovascular
Decision
Unknown
Applicant
Spectranetics, Inc.
Date Received
June 25, 2021
Decision Date
December 21, 2021
Product Code
QRJ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QRJ Laser-Powered Inferior Vena Cava Filter Retrieval Catheter

Other Clearances by Spectranetics, Inc.

K Number Device Name
K223472 TightRail Guardian Motorized Dilator Sheath, 9 French (575-009); TightRail Guardian Motorized Dilator Sheath, 11 French (575-011); TightRail Guardian Motorized Dilator Sheath, 13 French (575-013)
K222837 Turbo-Power (2.0mm) Laser Atherectomy Catheters, Turbo-Power (2.3mm) Laser Atherectomy Catheters
K212784 TightRail Guardian Motorized Dilator Sheath
K203540 Bridge Occlusion Balloon
K180694 Turbo-Power (2.0mm) Laser Atherectomy Catheters, Turbo-Power (2.3mm) Laser Atherectomy Catheters
K172687 Turbo-Power (2.0mm) Laser Atherectomy Catheters, Turbo-Power (2.3mm) Laser Atherectomy Catheters
K170059 Spectranetics Turbo-Elite Laser Atherectomy Catheters
K162561 Turbo-Power (2.0mm) Laser Atherectomy Catheters
K161333 TightRail Sub-C Rotating Dilator Sheath
K153530 Bridge Occlusion Balloon
Search all 17 clearances from Spectranetics, Inc. →