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

Pocguide Multi-Drug Test Panel, Pocguide Multi-Drug Test Panel OTC

K Number: K242498 · Decision Oct 1, 2024
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
29
Applicant Total
2
Review Days
40

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
Pocguide Multi-Drug Test Panel, Pocguide Multi-Drug Test Panel OTC
K Number
K242498
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3100
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aicheck Biotech, Inc.
Date Received
August 22, 2024
Decision Date
October 1, 2024
Product Code
NFT
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
NFT Test, Amphetamine, Over The Counter

Similar 510(k) Clearances

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

View all

Other Clearances by Aicheck Biotech, Inc.

K Number Device Name
K242077 PocguideTM Multi-Drug Test Cup OTC, PocguideTM Multi-Drug Test Cup