510(k) K961508
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