510(k) K101059
K101059 is an FDA 510(k) premarket notification submitted by Omega Laboratories, Inc. for the device "OMEGA LABORATORIES HAIR DRUG SCREENING ASSAY FOR PHENCYCLIDINE". The FDA issued a decision of Substantially Equivalent on July 12, 2010. The device falls under product code LCM (Enzyme Immunoassay, Phencyclidine), a Class U device. Omega Laboratories, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 12, 2010
- Date Received
- April 15, 2010
- 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