510(k) K871541

MARTIN-LEWIS AGAR W/REDUCED VANCOMYCIN C0226 by Gibco Laboratories Life Technologies, Inc. — Product Code JTY

K871541 is an FDA 510(k) premarket notification submitted by Gibco Laboratories Life Technologies, Inc. for the device "MARTIN-LEWIS AGAR W/REDUCED VANCOMYCIN C0226". The FDA issued a decision of Substantially Equivalent on April 29, 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. Gibco Laboratories Life Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 29, 1987
Date Received
April 20, 1987
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