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

THROMBO TEK PSE, MODEL 90-480

K Number: K082631 · Decision Dec 17, 2008
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
189
Applicant Total
10
Review Days
98

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
THROMBO TEK PSE, MODEL 90-480
K Number
K082631
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7290
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
R2 Diagnostics, Inc.
Date Received
September 10, 2008
Decision Date
December 17, 2008
Product Code
GGP
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
GGP Test, Qualitative And Quantitative Factor Deficiency

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GGP), ordered by most recent decision date.

View all

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
K062306 PLASMACON N, PLASMACON L-1, PLASMACON L-2
K050817 T-TEK
K042919 FIBROTEK FIB
K040296 PHOSPHOPLASTIN RL
K033471 PHOSPHOLIN ES AND CALCIUM CHLORIDE