510(k) K934467
K934467 is an FDA 510(k) premarket notification submitted by Beckman-Diagnostic Systems Group for the device "BECKMAN CX AMMONIA/ALCOHOL CONTROL". The FDA issued a decision of Substantially Equivalent on October 27, 1993. The device falls under product code DKC (Alcohol Control Materials), a Class I device regulated under 21 CFR 862.3280. Beckman-Diagnostic Systems Group has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 27, 1993
- Date Received
- September 10, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Alcohol Control Materials
- Device Class
- Class I
- Regulation Number
- 862.3280
- Review Panel
- TX
- Submission Type