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

T-TEK

K Number: K050817 · Decision Dec 12, 2005
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
19
Applicant Total
10
Review Days
256

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Basic Information

Device Name
T-TEK
K Number
K050817
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7875
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
R2 Diagnostics, Inc.
Date Received
March 31, 2005
Decision Date
December 12, 2005
Product Code
GJA
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
GJA Test, Thrombin Time

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Other Clearances by R2 Diagnostics, Inc.

K Number Device Name
K102908 NOFACT IX
K102851 NOFACT VIII
K090105 LUPOTEK KCT
K083878 LUPOTEK CORRECTIN VL, LUPOTEK DETECTIN VL, PLASMACON LA
K082631 THROMBO TEK PSE, MODEL 90-480
K062306 PLASMACON N, PLASMACON L-1, PLASMACON L-2
K042919 FIBROTEK FIB
K040296 PHOSPHOPLASTIN RL
K033471 PHOSPHOLIN ES AND CALCIUM CHLORIDE