510(k) K925970

MODEL 3D3 OSMOMETER by Advanced Instruments, Inc. — Product Code JJM

K925970 is an FDA 510(k) premarket notification submitted by Advanced Instruments, Inc. for the device "MODEL 3D3 OSMOMETER". The FDA issued a decision of Substantially Equivalent on July 9, 1993. 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
July 9, 1993
Date Received
November 25, 1992
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