510(k) K232192
- Device
- Venus Versa PRO System
- Applicant
- Venus Concept, Inc.
- 510(k) number
- K232192
- Product code
- ONF
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2023-09-11
- Date received
- 2023-07-24
- Regulation
- 878.4810
- Classification name
- Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
- Medical specialty
- General, Plastic Surgery
- Review panel
- General, Plastic Surgery
- Device class
- 2
- Clearance type
- Special
- Statement or summary
- Summary
- Third party reviewed
- No
Related Records
Applicant Contact
- Contact
- William H. McGrail
- Address
- 1800 Bering Dr. San Jose CA US 95112 95112
FDA Registration Numbers
- 3009736547
- 3010511300
- 3041275224
- 3007238544
- 3008442971
- 3006555617
- 3043657394
- 3009040934
- 3026540840
- 3043655996
- 3012133441
- 3004635398
- 3025104654
- 3006515340
- 3032147807
- 3012799115
- 3008915316
- 2953696
- 3021011208
- 3043047259
- 3033482500
- 3033884002
- 3010912900
- 3021349626
- 3033273466
- 9680762
- 3004069780
- 3033715699
- 3005238200
- 3015452693
- 3010273872
- 3016076698
- 3030230686
- 3006716777
- 3002808227
- 1313525
- 8040564
- 3011964664
- 3010902869
- 3016661372
- 3017905264
- 3021334828
- 3005695724
- 3011782009
- 3005855240
- 3025606176
- 3027645761
- 3027605738
- 3043011436
- 3009019578
- 3012772112
- 3022327202
- 3016496662
- 3009444646
- 3033891767
- 3037874486
- 3007113239
- 3034246188
- 3013494333
- 3011670002
- 3007120647
- 3033793026
- 3001431138
- 3006580954
- 3017619615
- 3033844600
- 3034995492
- 3043140693
- 3038715747
- 3006985163
- 3008925277
- 3023281259
- 3009488834
- 3027725665
- 3003542872
- 3011307265
- 2031934
- 3043012240
- 1222304
- 3007085226
Source Documents
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