510(k) K983510
K983510 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "CHEMSTRIP 101 URINE ANALYZER". The FDA issued a decision of Substantially Equivalent on October 27, 1998. The device falls under product code KQO (Automated Urinalysis System), a Class I device regulated under 21 CFR 862.2900. Boehringer Mannheim Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 27, 1998
- Date Received
- October 7, 1998
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Automated Urinalysis System
- Device Class
- Class I
- Regulation Number
- 862.2900
- Review Panel
- CH
- Submission Type