FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Distinct® Digital Pregnancy Test

K Number: K232715 · Decision May 31, 2024
Classifications
1
FEI Numbers
124
Registration Numbers
124
Same Product Code
223
Applicant Total
11
Review Days
269

Basic Information

Device Name
Distinct® Digital Pregnancy Test
K Number
K232715
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ACON Laboratories, Inc.
Date Received
September 5, 2023
Decision Date
May 31, 2024
Product Code
LCX
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
LCX Kit, Test, Pregnancy, Hcg, Over The Counter

Similar 510(k) Clearances

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

View all

Other Clearances by ACON Laboratories, Inc.

K Number Device Name
K250377 Flowflex Plus COVID-19 + Flu A/B Home Test
K230828 Flowflex COVID-19 Antigen Home Test
K192175 On Call Express II Blood Glucose Monitoring System
K191038 On Call Express Voice Blood Glucose Monitoring System
K181527 On Call Sure Blood Glucose Monitoring System, On Call Sure Sync Blood Glucose Monitoring System
K180504 Mission Lipid Panel Monitoring System
K180196 On Call Express Mobile Blood Glucose Monitoring System
K170587 On Call Ketone Reagent Strips for Urinalysis, Healthy Me Ketone Reagent Strips for Urinalysis
K151595 On Call Express Pro Blood Glucose Monitoring System
K150330 Mission Urinalysis Reagent Strips (Microalbumin/Creatinine)
Search all 11 clearances from ACON Laboratories, Inc. →