510(k) K864926
K864926 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "EMDS TM PHENOBARBITAL(PHNO) TESTPACK, #67677/95". The FDA issued a decision of Substantially Equivalent on January 7, 1987. The device falls under product code DLZ (Enzyme Immunoassay, Phenobarbital), a Class II device regulated under 21 CFR 862.3660. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 7, 1987
- Date Received
- December 16, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Immunoassay, Phenobarbital
- Device Class
- Class II
- Regulation Number
- 862.3660
- Review Panel
- TX
- Submission Type