510(k) K983255

MODIFICATION TO: PREMIER PLATINUM HPSA by Meridian Diagnostics, Inc. — Product Code LYR

K983255 is an FDA 510(k) premarket notification submitted by Meridian Diagnostics, Inc. for the device "MODIFICATION TO: PREMIER PLATINUM HPSA". The FDA issued a decision of Substantially Equivalent on December 17, 1998. The device falls under product code LYR (Helicobacter Pylori), a Class I device regulated under 21 CFR 866.3110. Meridian Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 17, 1998
Date Received
September 15, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Helicobacter Pylori
Device Class
Class I
Regulation Number
866.3110
Review Panel
MI
Submission Type