FDA.reportPublic FDA data

SANJIV KUMAR

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
96147093009384766SANJIV KUMAR1N2026-01-012015 Production Drive Apex NC US 27539
30048990053004899005SANJIV KUMAR1N2026-01-012015 Production Dr Apex NC US 27539
30083880053008388005Sanjiv Kumar1N2026-01-012015 Production Drive Apex NC US 27539
30097464253009746425Sanjiv Kumar1N2026-01-012015 Production Drive Apex NC US 27539
30157240783015724078Sanjiv Kumar1N2026-01-012015 PRODUCTION DR APEX NC US 27539
30157265513015731627Sanjiv Kumar1N2026-01-012015 Production Drive -- Apex NC US 27539

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
182261784345324K990519PHOENIX EPIDURAL & SPINAL NEEDLESBSP2000-06-02
2847641385326562K953252DISPOSABLE SCALP VEIN INFUSION SETFOZ1996-11-26
2847641074844035K945225DISPOSABLE SYRINGES AND DISPOSABLE NEEDLESFMF1995-01-26
1440012003841521K192679Sterile Syringe with Safety needle for Single Use, Sterile Syringe for Single Use, Sterile Safety Needle for Single UseMEG2020-04-10
1440011786396112K170276Safety Blood Collection Device for Single UseFMI2017-12-11
2847642017282723K000592UNOLOK PLUS INFUSION SET AND VAKU-8 PLUS BLOOD COLLECTION SETFPA2001-04-12
235751644259263
1440011984311380
182261276577106
1167831538832762
235751581590285
1167831634894373
1167831771827240
1167831855359657
2847641910697798
1167831945355730
2297981983232675

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MEG12020-04-10
FMI12017-12-11
FPA12001-04-12
BSP12000-06-02
FOZ11996-11-26
FMF11995-01-26