510(k) K864252

THAYER-MARTIN JEMBEC by Mds Laboratories, Inc. — Product Code JTY

K864252 is an FDA 510(k) premarket notification submitted by Mds Laboratories, Inc. for the device "THAYER-MARTIN JEMBEC". The FDA issued a decision of Substantially Equivalent on March 31, 1987. The device falls under product code JTY (Culture Media, For Isolation Of Pathogenic Neisseria), a Class II device regulated under 21 CFR 866.2410. Mds Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 31, 1987
Date Received
October 28, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Culture Media, For Isolation Of Pathogenic Neisseria
Device Class
Class II
Regulation Number
866.2410
Review Panel
MI
Submission Type