FDA.reportPublic FDA data

KOWA CO. LTD. CHOFU

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30112237513011223751KOWA CO. LTD. CHOFU1N2026-01-013-1, Chofugaoka 3-chome Chofu Tokyo JP 182-0021

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1747541094070775K960924KOWA HAND-HELD APPLANATION TONOMETER HA-1HKY1996-06-04
1747541508456970K261255KOWA FM-600MYC2026-09-11
1747541338109315K222372
1747541175065784K191945KOWA nonmyd 8HKI2019-09-10
1747541409789741K190573KOWA DR-1aHKI2019-06-04
1747541952786190K190056KOWA VK-2sNFJ2019-02-12
1747541178656279K133755KOWA SL-17HJO2014-03-11
1747541674153654K112330KOWA VX-20HKI2012-02-16
1747541950221022K101628KOWA NONMYD WXHKI2011-01-26
1747542066217060K091683KOWA VX-10 AHKI2009-07-02
1747541704017039K091098KOWAGENESIS-DFHKI2009-08-07
1747541300685115K091039KOWA, FM-600, MODEL LSS50MYC2009-08-07
1747541536680578K050271KOWA GENESIS-D HAND-HELD RETINAL CAMERAHKI2005-11-03
1747541704913110
1747541643544254

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
HKI72019-09-10
MYC22026-09-11
NFJ12019-02-12
HJO12014-03-11
HKY11996-06-04

PMN#