FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112

K Number: K040575 · Decision May 20, 2004
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
87
Applicant Total
15
Review Days
77

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112
K Number
K040575
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Phamatech, Inc.
Date Received
March 4, 2004
Decision Date
May 20, 2004
Product Code
CGJ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CGJ Radioimmunoassay, Follicle-Stimulating Hormone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CGJ), ordered by most recent decision date.

View all

Other Clearances by Phamatech, Inc.

K Number Device Name
K181945 QuickScreen Pro Multi Drug Screening Test, Model 9395Z
K131069 QUICKSCREEN AMPHETINE 500 TEST
K103295 QUICKSCREEN COCAINE 150 SCREENING TEST
K070009 AT HOME DRUG TEST MODELS, 9308T AND 9308X
K070098 QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018; MULTI DRUG SCREENING TEST, MODEL 9317T; CUP MULTI DRUG SC
K043599 MOMENTS MENOPAUSE CHECK, MODEL 9113
K043051 QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121
K043167 PHAMATECH QUICKSCREEN BENZODIAZEPINES TEST, MODELS 9025, 9026, 9027T, 9153T AND 9195X
K021409 AT HOME OVULATION TEST, MODEL 9032
K013408 AT HOME DRUG TEST, MODEL 9079
Search all 15 clearances from Phamatech, Inc. →