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

Amplichek I, Negative , Amplichek I, Level 1, Amplichek I, Level 2, Amplichek I, Level 3, Amplichek I, MiniPak

K Number: K152679 · Decision May 10, 2016
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
30
Applicant Total
46
Review Days
235

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Basic Information

Device Name
Amplichek I, Negative , Amplichek I, Level 1, Amplichek I, Level 2, Amplichek I, Level 3, Amplichek I, MiniPak
K Number
K152679
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3920
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio-Rad Laboratories
Date Received
September 18, 2015
Decision Date
May 10, 2016
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

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