510(k) K971600
K971600 is an FDA 510(k) premarket notification submitted by Behring Diagnostics, Inc. for the device "EMIT CALIBRATOR B LEVEL 1 (CUTOFF)/EMIT CALIBRATOR B LEVEL 2 (HIGH)". The FDA issued a decision of Substantially Equivalent on June 25, 1997. The device falls under product code DKB (Calibrators, Drug Mixture), a Class II device regulated under 21 CFR 862.3200. Behring Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 25, 1997
- Date Received
- May 1, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Calibrators, Drug Mixture
- Device Class
- Class II
- Regulation Number
- 862.3200
- Review Panel
- TX
- Submission Type