510(k) K162620

Remel Spectra ESBL by Remel, Inc. — Product Code JSO

K162620 is an FDA 510(k) premarket notification submitted by Remel, Inc. for the device "Remel Spectra ESBL". The FDA issued a decision of Substantially Equivalent on May 1, 2017. The device falls under product code JSO (Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar), a Class II device regulated under 21 CFR 866.1700. Remel, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 1, 2017
Date Received
September 20, 2016
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar
Device Class
Class II
Regulation Number
866.1700
Review Panel
MI
Submission Type