Last synced on 20 December 2024 at 11:05 pm

Automated System For Sample Preparation And Identification Of Microorganisms From Cultured Isolates By Mass Spectrometry

Page Type
Product Code
Definition
An automated in vitro diagnostic system to prepare colonies of microorganisms grown on solid culture media from human specimens for qualitative identification and differentiation using matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS).
Physical State
In vitro diagnostic device
Technical Method
Matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) microorganism identification
Target Area
Identification and differentiation of microorganisms cultured from human specimens
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3378
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 QQV is linked to regulation 21CFR866.3378, which does not seem to exist yet. It may be pending at the moment.

Automated System For Sample Preparation And Identification Of Microorganisms From Cultured Isolates By Mass Spectrometry

Page Type
Product Code
Definition
An automated in vitro diagnostic system to prepare colonies of microorganisms grown on solid culture media from human specimens for qualitative identification and differentiation using matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS).
Physical State
In vitro diagnostic device
Technical Method
Matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) microorganism identification
Target Area
Identification and differentiation of microorganisms cultured from human specimens
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3378
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 QQV is linked to regulation 21CFR866.3378, which does not seem to exist yet. It may be pending at the moment.