510(k) K992268
- Device
- Nac Prn Needleless Access Connector
- Applicant
- THE KIPP GROUP
- 510(k) number
- K992268
- Product code
- FPA
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1999-09-15
- Date received
- 1999-07-06
- Regulation
- 880.5440
- Classification name
- Set, Administration, Intravascular
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Statement
- Third party reviewed
- No
Related Records
Applicant Contact
- Contact
- TIM L TRUITT
- Address
- 930 Wanamaker Ave. Ontario CA US 91761 91761
FDA Registration Numbers
- 3017262697
- 3002806818
- 1423537
- 1221765
- 1063851
- 1024879
- 3011987967
- 3003674698
- 1526611
- 8041145
- 3034669683
- 2024064
- 3013696225
- 3011642792
- 8040700
- 9616099
- 3005778453
- 9680306
- 3003974574
- 3015997711
- 1047843
- 2032521
- 2433012
- 3005458990
- 1054241
- 1928237
- 9612057
- 3007616112
- 1410248
- 9681835
- 9611665
- 9610847
- 3017567825
- 9610825
- 3010149039
- 1220477
- 9615050
- 1019003
- 3010273872
- 3018229072
- 3022964615
- 1016427
- 9612051
- 3022699058
- 2243072
- 3007344957
- 3016472589
- 3007363456
- 1820334
- 1422078
- 1417485
- 3004911384
- 1061124
- 3012187635
- 3010293992
- 1526863
- 3012410077
- 3017509841
- 3008448733
- 3030733800
- 9610993
- 3016904853
- 2320762
- 3008782867
- 3015140199
- 3012104670
- 1424263
- 3019807891
- 3010381606
- 3020417125
- 3015724078
- 3017961114
- 3005934752
- 2032098
- 3012429465
- 3012969104
- 9681572
- 1038185
- 3005669815
Source Documents
510(k) summary PDF not indicated by FDA
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