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

PHOSPHORUS TEST (PHOS) ITEM NUMBER 65416

K Number: K945322 · Decision Dec 7, 1994
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
62
Review Days
36

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Basic Information

Device Name
PHOSPHORUS TEST (PHOS) ITEM NUMBER 65416
K Number
K945322
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Emd Chemicals, Inc.
Date Received
November 1, 1994
Decision Date
December 7, 1994
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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K951494 AMYLASE TEST ITEM 97381/94 (R1, 97382/94 (R2-SR)
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K950234 TOTAL PROTEIN TEST (TPRO) ITEM NUMBER: XXXXX/R1. R2
K950128 TOTAL PROTEIN TEST (TPRO) ITEM XXXXX/R1. R2
K945368 PHOSPHORUS TEST (PHOS)
K840883 UNIPAK 100 ANALYZER, 65156 & CHEMISTR
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