510(k) K222579
- Device
- Belun Sleep System BLS-100
- Applicant
- Belun Technology Company Limited
- 510(k) number
- K222579
- Product code
- MNR
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2023-02-23
- Date received
- 2022-08-25
- Regulation
- 868.2375
- Classification name
- Ventilatory Effort Recorder
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- N
- Source
- FDA openFDA 510(k) dataset plus migrated FDA.report data
Related Records
Applicant Contact
- Contact
- Leung Lap Wai Lydia
- Address
- Unit 218, 2/F, Core Bldg. 2, # 1 Science Park West Ave., Hong Kong Science Park Sha Tin CN
FDA Registration Numbers
- 3036722175
- 3004604967
- 1423640
- 3006463573
- 3004428458
- 9613619
- 3009001657
- 3009770872
- 3018783526
- 1529102
- 8044004
- 3004531588
- 3010399798
- 1063925
- 3007799743
- 3012302888
- 3011120183
- 9615102
- 3017638059
- 3010157426
- 3015529350
- 3020283264
- 3038274470
- 3006258337
- 3008208119
- 1118193
- 3016998644
- 3011782009
- 3010175098
- 2518422
- 3007616088
- 3003832357
- 1650946
- 1417592
- 3007583504
- 3013689228
- 3004016520
- 9611295
- 3012305175
- 3033715634
- 3004964738
- 3011205710
- 3020018
- 3006125362
- 3017684630
- 3000126629
- 3005873568
- 3008820594
- 3007389703
- 3004748541
- 2184161
- 3011061417
- 3033526676
- 3024722701
- 3010272829
- 3003616071
- 3023272766
- 3026753386
- 3013724298
- 3024891505
- 3002912391
- 1314417
- 3002736372
- 3038185755
- 3002797442
- 3009351773
- 3002806730
- 3006606984
- 3007573469
- 3008253300
- 3016939722
- 3018117195
- 9614500
- 3006606827
- 2011171
- 3032906215
- 9617286
- 9612330
- 3009498109
- 3022315836
- 3005581270
- 2132556
Source Documents
FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON
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