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

NATtrol BD MAX Vaginal Panel External Controls

K Number: K201403 · Decision Feb 2, 2022
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
30
Applicant Total
1
Review Days
615

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
NATtrol BD MAX Vaginal Panel External Controls
K Number
K201403
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3920
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zeptometrix
Date Received
May 28, 2020
Decision Date
February 2, 2022
Product Code
PMN
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
PMN Assayed External Control Material For Microbiology Nucleic Acid Amplification (Nat) Assays

Similar 510(k) Clearances

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

View all