510(k) K000399
K000399 is an FDA 510(k) premarket notification submitted by OraSure Technologies, Inc. for the device "STC PCP INTERCEPT MICRO-PLATE EIA, MODEL 11541". The FDA issued a decision of Substantially Equivalent on May 15, 2000. 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
- May 15, 2000
- Date Received
- February 7, 2000
- 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