FDA.reportPublic FDA data

PHAMATECH INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
20312293000719950PHAMATECH INC.1N2026-01-0115175 Innovation Dr San Diego CA US 92128

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00674033090682At Home Drug Test for Methamphetamine - Urine based drug testing device for Methamphetamine877-466-3837athomedrugtest@phamatech.com
00674033090736At Home Single Panel COC + Timer - Single Panel Cocaine urine drug test device with Timer877-466-3837athomedrugtest@phamatech.com
00674033090781At Home Drug Test for Marijuana - Urine based drug of abuse test for THC877-466-3837athomedrugtest@phamatech.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
825711847155582K993141AT HOME QUICKCUP PREGNANCY TEST, MODEL 9015LCX1999-11-08
825711502610344K990249OVUSTICK LH OVULATION PREDICTOR, MODEL 9030, OVUCARD LH OVULATION PREDICTOR, MODEL 9031CEP1999-03-22
825711538067690K982938QUICK SCREEN METHADONE SCREENING TEST, MODELS 9035, 9036, QUICK SCREEN PRO MULTI DRUG SCREENING TEST MODEL 9153DJR1999-02-05
825711111168170K974615QUICKSTICK PRO HCG TESTJHI1998-01-26
825711578992899K974582QUICKSCREEN ONE STEP PCP SCREENING TESTLCM1998-02-04
825711532351413K973122QUICKSCREEN ONE STEP THC SCREENING TESTLDJ1997-09-25
825711115824859K972619QUICKSCREEN ONE STEP OPIATE SCREENING TEST (9080)DJG1997-08-20
825711799332869K972618QUICKSCREEN ONE STEP COCAINE SCREENING TEST (9070)DMN1997-08-08
825711255671623K972577QUICK SCREEN ONE STEP AMPHETAMINE TESTDIT1997-08-20
825711952929531K972556QUICKSCREEN ONE STEP METHAMPHETAMINE TEST(9065)LAF1997-09-02
825711282729560K070098QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018; MULTI DRUG SCREENING TEST, MODEL 9317T; CUP MULTI DRUG SCDIS2007-12-07
825711224946106K070009AT HOME DRUG TEST MODELS, 9308T AND 9308XDIS2007-12-07
825711965682082K043167PHAMATECH QUICKSCREEN BENZODIAZEPINES TEST, MODELS 9025, 9026, 9027T, 9153T AND 9195XJXM2004-12-29
825711296864502K043051QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121DJG2005-02-07
825711868550531K040575PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112CGJ2004-05-20
825711710500230K003858MODIFICATION TO AT HOME DRUG TEST, MODELS 9150, 9068, AND 9175MVO2001-02-12
825711266693324
825711534775787

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
DIS22007-12-07
DJG22005-02-07
JXM12004-12-29
CGJ12004-05-20
MVO12001-02-12
LCX11999-11-08
CEP11999-03-22
DJR11999-02-05
LCM11998-02-04
JHI11998-01-26
LDJ11997-09-25
LAF11997-09-02
DIT11997-08-20
DMN11997-08-08

PMN#

55 records. Showing 1-40. Next

GUDID#