FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

QUIDEL HELICOBACTER PYLORI POSTIVE/NEGATIVE CONTR

K Number: K905049 · Decision May 7, 1991
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
90
Applicant Total
93
Review Days
180

Basic Information

Device Name
QUIDEL HELICOBACTER PYLORI POSTIVE/NEGATIVE CONTR
K Number
K905049
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3110
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
QUIDEL CORP.
Date Received
November 8, 1990
Decision Date
May 7, 1991
Product Code
LYR
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
LYR Helicobacter Pylori

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