510(k) K874272
K874272 is an FDA 510(k) premarket notification submitted by Roche Diagnostic Systems, Inc. for the device "REVISED LABELING FOR METHAQUALONE TEST KIT". The FDA issued a decision of Substantially Equivalent on November 13, 1987. The device falls under product code KXS (Radioimmunoassay, Methaqualone), a Class II device regulated under 21 CFR 862.3630. Roche Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 13, 1987
- Date Received
- October 20, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Methaqualone
- Device Class
- Class II
- Regulation Number
- 862.3630
- Review Panel
- TX
- Submission Type