510(k) K911092

OSMOMETER MODEL 2400 by Advanced Instruments, Inc. — Product Code JJM

K911092 is an FDA 510(k) premarket notification submitted by Advanced Instruments, Inc. for the device "OSMOMETER MODEL 2400". The FDA issued a decision of Substantially Equivalent on May 22, 1991. 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
May 22, 1991
Date Received
March 11, 1991
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