510(k) K902409
- Device
- Becton Dickinson 360 Infuser (tm) System
- Applicant
- BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
- 510(k) number
- K902409
- Product code
- FRN
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1990-07-19
- Date received
- 1990-05-31
- Regulation
- 880.5725
- Classification name
- Pump, Infusion
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- N
- Source
- FDA openFDA 510(k) dataset plus migrated FDA.report data
Related Records
Applicant Contact
- Contact
- J ARNSBERGER
- Address
- 1 Becton Dr. Franklin Lakes NJ US 07417 07417
FDA Registration Numbers
- 2521402
- 3011883032
- 1423507
- 3006575795
- 1416980
- 2650143
- 1061124
- 3000240707
- 1054713
- 3010291427
- 3008132411
- 9615908
- 2032098
- 1018470
- 2027804
- 1220973
- 3000204189
- 1219702
- 3013557562
- 1125615
- 3003879246
- 1319660
- 1423537
- 1000163068
- 3016798778
- 3012307300
- 3024122953
- 3013298431
- 3017636737
- 1045254
- 3008692839
- 3012302888
- 3012337868
- 9681819
- 3009456923
- 3008810357
- 3005382983
- 9710049
- 3006158088
- 2032227
- 3004530184
- 3005627859
- 3010564249
- 3015158050
- 1066270
- 3006534321
- 9614279
- 3002808022
- 9680741
- 3008058400
- 3013319212
- 3016509758
- 3013722099
- 3029973819
- 1058584
- 3004548776
- 3007738736
- 3008570882
- 3003927385
- 3018229072
- 1526611
- 2022994
- 2024064
- 1723170
- 1713468
- 2029015
- 3004906872
- 1121996
- 1928237
- 2411512
- 1319639
- 3004112621
- 1420032
- 9615050
- 3010082909
- 3005778453
- 9610825
- 3014732157
- 2024022
- 1314492
Source Documents
FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON
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