Falloposcope

Device Code: 4016

Product Code(s): MKO

Device Classification Information

• Device Type ID: 4016
• Device Name: Falloposcope
• Regulation Description: Hysteroscope And Accessories.
• Regulation Medical Specialty: Obstetrics/Gynecology
• Review Panel: Obstetrics/Gynecology
• Premarket Review: Office Of Device Evaluation (ODE); Division Of Reproductive, Gastro-Renal, And Urological Devices (DRGUD); Obstetrics And Gynecology Devices Branch (OGDB)
• Submission Type: 510(k)
• CFR Regulation Number: 884.1690 [🔎]
• FDA Device Classification: Class 2 Medical Device
• Product Code: MKO
• GMP Exempt: No
• Summary MR: Eligible
• Implanted Device: No
• Life Support Device: No
• Third Party Review: Not Third Party Eligible

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: 4016
• Device: Falloposcope
• Product Code: MKO
• FDA Device Classification: Class 2 Medical Device
• Regulation Description: Hysteroscope And Accessories.
• CFR Regulation Number: 884.1690 [🔎]

TPLC Last Update: 2019-04-02 20:41:42