510(k) K961221

PYLORI IGG ELISA TEST SYSTEM by Armkel, LLC — Product Code LYR

K961221 is an FDA 510(k) premarket notification submitted by Armkel, LLC for the device "PYLORI IGG ELISA TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on July 30, 1996. The device falls under product code LYR (Helicobacter Pylori), a Class I device regulated under 21 CFR 866.3110. Armkel, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 30, 1996
Date Received
March 20, 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