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

NATURAL DETECTOR SYSTEM

K Number: K861731 · Decision Nov 6, 1986
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
96
Applicant Total
2
Review Days
184

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Basic Information

Device Name
NATURAL DETECTOR SYSTEM
K Number
K861731
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.6550
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
U.S. Health Resources Corp.
Date Received
May 6, 1986
Decision Date
November 6, 1986
Product Code
KHE
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KHE Reagent, Occult Blood

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Other Clearances by U.S. Health Resources Corp.

K Number Device Name
K861452 MONOSTAR SYSTEM: IM LATEX TEST