FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MODEL 3D3 OSMOMETER

K Number: K925970 · Decision Jul 9, 1993
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
11
Applicant Total
16
Review Days
226

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Basic Information

Device Name
MODEL 3D3 OSMOMETER
K Number
K925970
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2730
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Advanced Instruments, Inc.
Date Received
November 25, 1992
Decision Date
July 9, 1993
Product Code
JJM
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JJM Osmometer For Clinical Use

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Other Clearances by Advanced Instruments, Inc.

K Number Device Name
K152776 Glocyte Automated Cell Counter System
K120631 PATIENT MONITOR
K112465 VITAL SIGNS MONITOR
K965036 THE ADVANCED OSMOMETER (3900)
K962056 ADVANCED MICRO-OSMOMETER MODEL 3300
K930526 INTERMITTENT COMPRESSION SYSTEM MODEL 5000
K911092 OSMOMETER MODEL 2400
K873642 OSMOMETER MODEL 110
K863516 ELECTRONIC METAL LOCATOR MODEL MD-1
K842784 CEREGROTRAC
Search all 16 clearances from Advanced Instruments, Inc. →