510(k) K961508

IMMUNOCARD H. PYLORI by Meridian Diagnostics, Inc. — Product Code LYR

K961508 is an FDA 510(k) premarket notification submitted by Meridian Diagnostics, Inc. for the device "IMMUNOCARD H. PYLORI". The FDA issued a decision of Substantially Equivalent on January 21, 1997. 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
January 21, 1997
Date Received
April 19, 1996
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