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

SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL

K Number: K010598 · Decision Mar 23, 2001
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
191
Applicant Total
38
Review Days
23

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Basic Information

Device Name
SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL
K Number
K010598
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.8625
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quantimetrix Corp.
Date Received
February 28, 2001
Decision Date
March 23, 2001
Product Code
JPK
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
JPK Mixture, Hematology Quality Control

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