510(k) K983510

CHEMSTRIP 101 URINE ANALYZER by Boehringer Mannheim Corp. — Product Code KQO

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