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

KSEA DION-GRACIA SET

K Number: K010785 · Decision Aug 21, 2001
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
334
Review Days
159

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Basic Information

Device Name
KSEA DION-GRACIA SET
K Number
K010785
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KARL STORZ Endoscopy-America, Inc.
Date Received
March 15, 2001
Decision Date
August 21, 2001
Product Code
DXC
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
DXC Clamp, Vascular

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Other Clearances by KARL STORZ Endoscopy-America, Inc.

K Number Device Name
K252624 KARL STORZ Laryngoscopes and Accessories
K223923 HOPKINS Telescopes
K202957 Flexible Video Cysto-Urethroscope (C-view)
K200318 UNIDRIVE S II ENT, DrillCut-X II-35 Shaver Handpiece, DrillCut-X II-35 N Shaver Handpiece
K201135 Image1 S CCU, Image1 S 4U Camera Head
K200740 HD Video Rhino Laryngoscope
K191357 Flexible HD Cysto-Urethroscope System
K182723 Flexible HD Cysto-Urethroscope System
K182186 CMOS Video-Rhino-Laryngoscope System
K183264 Flex-THOR scope
Search all 334 clearances from KARL STORZ Endoscopy-America, Inc. →