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Precision Medical Devices Inc

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30074787143007478714Precision Medical Devices Inc1Y2026-01-01121 Jersey Ave Suite 203 New Brunswick NJ US 08901

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1113801356261278K061065FECAL OCCULT BLOOD CARD TEST, MODEL F735-A, FECAL OCCULT BLOOD CARD KIT, MODEL F735-25KHE2006-07-14
1113801260490132DEN200001Cell-Free DNA BCTQMA2020-08-07
1113801005811406
1113801024568366
1113801226109270
1113801514339630
1113801083660695
1113801131037224
1113801292719328
1113801330668064
1113801398865876
1113801445033711
1113801532233310
1113801654894165
1113801685792993
1113801704448700
1113801728694528
1113801799187651
1113801805117503
1113801863883771
1113801890023375
1113801898171895
1113801933780502
1113802004393759

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
QMA12020-08-07
KHE12006-07-14