FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OSMOMETER STANDARD SOLUTIONS

K Number: K892329 · Decision Oct 31, 1989
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
5
Review Days
209

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Basic Information

Device Name
OSMOMETER STANDARD SOLUTIONS
K Number
K892329
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
D.R.G. Scientific Industries
Date Received
April 5, 1989
Decision Date
October 31, 1989
Product Code
JIT
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
JIT Calibrator, Secondary

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K Number Device Name
K870889 ACID FUCHSIN SOLUTIONS
K863880 BLOOD GASES/ PO2, PCO2 AND BLOOD PH ANALYSIS PROD.
K863825 CO-OXIMETER SOLUTIONS
K863824 SOLUTION/TEST STANDARD/CONDUCT. DIALY.&MULT.SOLUT.