510(k) K873642

OSMOMETER MODEL 110 by Advanced Instruments, Inc. — Product Code JJM

K873642 is an FDA 510(k) premarket notification submitted by Advanced Instruments, Inc. for the device "OSMOMETER MODEL 110". The FDA issued a decision of Substantially Equivalent on October 20, 1987. The device falls under product code JJM (Osmometer For Clinical Use), a Class I device regulated under 21 CFR 862.2730. Advanced Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 20, 1987
Date Received
September 9, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Osmometer For Clinical Use
Device Class
Class I
Regulation Number
862.2730
Review Panel
CH
Submission Type