Angioscope

Device Code: 998

Product Code(s): LYK

Device Classification Information

• Device Type ID: 998
• Device Name: Angioscope
• Regulation Description: Endoscope And Accessories.
• Regulation Medical Specialty: Gastroenterology/Urology
• Review Panel: Cardiovascular
• Premarket Review: Office Of Device Evaluation (ODE); Division Of Cardiovascular Devices (DCD); Interventional Cardiology Devices Branch (ICDB)
• Submission Type: 510(k)
• CFR Regulation Number: 876.1500 [🔎]
• FDA Device Classification: Class 2 Medical Device
• Product Code: LYK
• GMP Exempt: No
• Summary MR: Eligible
• Implanted Device: No
• Life Support Device: No
• Third Party Review: Eligible For Accredited Persons Expansion Pilot Program

Recognized Standards

• 9-39 ISO 8600-5 First Edition 2005-03-15
  Optics And Photonics - Medical Endoscopes And Endotherapy Devices - Part 5: Determination Of Optical Resolution Of Rigid Endoscopes With Optics
• 9-40 ISO 8600-6 First Edition 2005-03-15
  Optics And Photonics - Medical Endoscopes And Endotherapy Devices - Part 6: Vocabulary
• 9-84 ISO 8600-3 First Edition 1997-07-01 (Amendment 1 2003-12-01
  Optics And Optical Instruments - Medical Endoscopes And Endoscopic Accessories - Part 3: Determination Of Field Of View And Direction Of View Of Endoscopes With Optics [Including: Amendment 1 (2003)]
• 9-94 ISO 8600-4 Second Edition 2014-03-15
  Endoscopes - Medical Endoscopes And Certain Accessories - Part 4: Determination Of Maximum Width Of Insertion Portion
• 9-110 ISO 8600-1 Fourth Edition 2015-10-15
  Endoscopes - Medical Endoscopes And Endotherapy Devices -- Part 1: General Requirements

Total Product Life Cycle

• Device Type ID: 998
• Device: Angioscope
• Product Code: LYK
• FDA Device Classification: Class 2 Medical Device
• Regulation Description: Endoscope And Accessories.
• CFR Regulation Number: 876.1500 [🔎]

Device Problems
Blocked Connection	1
Total Device Problems	1

TPLC Last Update: 2019-04-02 19:46:01