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

BIOTROL INORGANIC PHOSPHORUS

K Number: K885041 · Decision Jan 30, 1989
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
46
Review Days
56

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Basic Information

Device Name
BIOTROL INORGANIC PHOSPHORUS
K Number
K885041
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Biotrol, USA, Inc.
Date Received
December 5, 1988
Decision Date
January 30, 1989
Product Code
CEO
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
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus

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Other Clearances by Biotrol, USA, Inc.

K Number Device Name
K934014 VACUSOL PLUS DENTAL VACUUM LINE CLEANER/DISINFECTANT
K931141 BIOTROL AMYLASE CNPG3
K921855 BIOTROL BICARBONATE STANDARDS
K921677 BIOTROL MAGNESIUM (MAGON)
K912795 BIOTROL UIBC REAGENT
K910721 BIOTROL PROTEIN MULTILEVEL STANDARDS
K905683 BIOTROL LACTATE DEHYDROGENASE (L-P)
K905280 BIOTROL BILIRUBIN C & T CONTROL
K894544 BIOTROL RUB-E.I.A. TEST G
K891061 BIOTROL CALCIUM MONOREACTIF
Search all 46 clearances from Biotrol, USA, Inc. →