Last synced on 10 January 2025 at 11:05 pm

Positive Blood Culture Processor For Inoculum Preparation Used For Antimicrobial Susceptibility Testing

Page Type
Product Code
Definition
Processing device that includes associated reagents, when applicable, that is intended to recover microbes from positive blood cultures for inoculum preparation. The prepared inoculum is intended for subsequent use in antimicrobial susceptibility testing.
Physical State
In vitro diagnostic device
Technical Method
Processor to prepare an inoculum for subsequent use in antimicrobial susceptibility testing.
Target Area
For antimicrobial susceptibility testing using an inoculum of microbial cells recovered from positive blood cultures.
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.1650
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QZX is linked to regulation 21CFR866.1650, which does not seem to exist yet. It may be pending at the moment.

Positive Blood Culture Processor For Inoculum Preparation Used For Antimicrobial Susceptibility Testing

Page Type
Product Code
Definition
Processing device that includes associated reagents, when applicable, that is intended to recover microbes from positive blood cultures for inoculum preparation. The prepared inoculum is intended for subsequent use in antimicrobial susceptibility testing.
Physical State
In vitro diagnostic device
Technical Method
Processor to prepare an inoculum for subsequent use in antimicrobial susceptibility testing.
Target Area
For antimicrobial susceptibility testing using an inoculum of microbial cells recovered from positive blood cultures.
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.1650
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QZX is linked to regulation 21CFR866.1650, which does not seem to exist yet. It may be pending at the moment.