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510(k) K182764

Biop Digital Colposcope by Biop Medical , Ltd. — Product Code HEX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 27, 2018
Date Received
September 28, 2018
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Colposcope (And Colpomicroscope)
Device Class
Class II
Regulation Number
884.1630
Review Panel
OB
Submission Type

Other clearances for product code HEX

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  • K190187 — Gynescope System (May 8, 2019)
  • K181034 — Pocket Colposcope System (September 21, 2018)
  • K170446 — LT-300 SD Digital Video Colposcope (May 21, 2017)
  • K161871 — EVA (Enhanced Visual Assessment) System (December 19, 2016)
  • K160341 — Colposcope System (September 14, 2016)
  • K160380 — LT-300 HD (May 13, 2016)
  • K151878 — Video Colposcope (December 1, 2015)
  • K143119 — LT-300 Video Colposcope (December 18, 2014)
  • K140754 — COOPER SURGICAL LEISEGANG COLPOSCOPE SYSTEM (October 23, 2014)