Sopro
Sopro holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2023.
Top product codes for Sopro
Recent clearances by Sopro
- K223470 — C50
- K121685 — SOPROCARE
- K103813 — SOPRO 281
- K092329 — SOPIX 2
- K092583 — SOPROLIFE
- K082796 — SOPRO 184 CAMERA
- K080122 — SOPRO 670 ARTHROSCOPIC PUMP
- K070783 — SOPRO MODEL 640 LAPAROSCOPIC INSUFFLATOR
- K072912 — SOPRO 225 DUAL HALOGEN LIGHT SOURCE
- K070102 — SOPRO 162 CAMERA
- K031593 — SOPRO 61D
- K020915 — SOPRO LIGHT SOURCES AND ACCESSORIES
- K020270 — SOPRO 367D 3CCD FULL DIGITAL ENDOSCOPY CAMERA
- K013090 — SOPRO 67D OPERATING ROOM CAMERA
- K012505 — SOPRO595 INTRA ORAL CAMERA
- K000422 — S57D DIGITAL OPERATING ROOM CAMERA
- K000423 — S52D DIGITAL VIDEO LAPAROSCOPE
- K000424 — S51D DIGITAL ENDOSCOPY CAMERA
- K990948 — S575 INTRAORAL DOCKING DENTAL CAMERA
- K983625 — S555 INTRAORAL DENTAL CAMERA
- K973794 — S-57 VIDEO IMAGING SYSTEM
- K973795 — S-52 ELECTRONIC VIDEO LAPAROSCOPE
- K973796 — S-41 &41S VIDEO IMAGING SYSTEM
- K973798 — S-357 VIDEO IMAGING SYSTEM
- K972540 — S-357 VIDEO IMAGING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.