510(k) K872056
K872056 is an FDA 510(k) premarket notification submitted by Boots-Celltech Diagnostics, Inc. for the device "MODIFIED (DIRECTIONS FOR USE) FOR IDEIA(TM) TEST". The FDA issued a decision of Substantially Equivalent on June 15, 1987. The device falls under product code LJC (Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)), a Class I device regulated under 21 CFR 866.3120. Boots-Celltech Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 15, 1987
- Date Received
- May 28, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)
- Device Class
- Class I
- Regulation Number
- 866.3120
- Review Panel
- MI
- Submission Type