510(k) K982801
K982801 is an FDA 510(k) premarket notification submitted by OraSure Technologies, Inc. for the device "AUTO-LYTE PCP EIA, MODEL #1254U". The FDA issued a decision of Substantially Equivalent on November 4, 1998. The device falls under product code LCM (Enzyme Immunoassay, Phencyclidine), a Class U device. OraSure Technologies, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 4, 1998
- Date Received
- August 10, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Immunoassay, Phencyclidine
- Device Class
- Class U
- Regulation Number
- Review Panel
- TX
- Submission Type