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

OSMOMETER MODEL 110

K Number: K873642 · Decision Oct 20, 1987
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
11
Applicant Total
16
Review Days
41

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Basic Information

Device Name
OSMOMETER MODEL 110
K Number
K873642
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2730
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Advanced Instruments, Inc.
Date Received
September 9, 1987
Decision Date
October 20, 1987
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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K Number Device Name
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K965036 THE ADVANCED OSMOMETER (3900)
K962056 ADVANCED MICRO-OSMOMETER MODEL 3300
K930526 INTERMITTENT COMPRESSION SYSTEM MODEL 5000
K925970 MODEL 3D3 OSMOMETER
K911092 OSMOMETER MODEL 2400
K863516 ELECTRONIC METAL LOCATOR MODEL MD-1
K842784 CEREGROTRAC
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