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

PHOPHORUS REAGNET SET

K Number: K841061 · Decision May 1, 1984
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
40
Review Days
50

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Basic Information

Device Name
PHOPHORUS REAGNET SET
K Number
K841061
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Medical Specialties, Inc.
Date Received
March 12, 1984
Decision Date
May 1, 1984
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 Medical Specialties, Inc.

K Number Device Name
K946201 STAND, INFUSION
K931947 CHECKPOINT
K926095 REFRACTROL-SP
K924926 MSI-HCT
K896566 MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE
K883703 MSI-CAL 7
K883851 MSI-CAL 8
K883850 MSI-CAL 16
K880608 MSI-PC
K880270 MSI-DIFF PLUS
Search all 40 clearances from Medical Specialties, Inc. →