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

QUIDEL MOLECULAR RSV + HMPV ASSAY

K Number: K131813 · Decision Sep 6, 2013
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
78
Applicant Total
93
Review Days
78

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
QUIDEL MOLECULAR RSV + HMPV ASSAY
K Number
K131813
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3980
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quidel Corp.
Date Received
June 20, 2013
Decision Date
September 6, 2013
Product Code
OCC
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
OCC Respiratory Virus Panel Nucleic Acid Assay System

Similar 510(k) Clearances

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

View all

Other Clearances by Quidel Corp.

K Number Device Name
K131728 QUIDEL MOLECULAR INFLUENZA A + B ASSAY
K130398 SOFIA(R) RSV FIA
K131166 SOFIA(R) HCG FIA
K131606 SOFIA INFLUENZA A+B FIA
K131619 QUICKVUE INFLUENZA A+B
K122189 QUIDEL MOLECULAR RSV + HMPV ASSAY
K123998 QUIDEL MOLECULAR DIRECT C. DIFFICILE ASSAY
K113777 QUIDEL MOLECULAR INFLUENZA A+B
K112172 QUIDEL MOLECULAR INFLUENZA A + B ASSAY
K112490 QUIDEL MOLECULAR HMPV ASSAY
Search all 93 clearances from Quidel Corp. →