510(k) K941425
K941425 is an FDA 510(k) premarket notification submitted by Alamar Biosciences Laboratory, Inc. for the device "ALAMAR ANTIBIOTIC SUSCEPTIBILITY". The FDA issued a decision of Substantially Equivalent on December 15, 1994. The device falls under product code LRG (Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems), a Class II device regulated under 21 CFR 866.1640. Alamar Biosciences Laboratory, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 15, 1994
- Date Received
- March 23, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems
- Device Class
- Class II
- Regulation Number
- 866.1640
- Review Panel
- MI
- Submission Type