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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device kit, quality control for blood banking reagents
Product CodeKSF
Regulation Number 864.9650
Device Class 2


Premarket Reviews
ManufacturerDecision
ALBA BIOSCIENCE LIMITED
  SUBSTANTIALLY EQUIVALENT 4
ALBA BIOSCIENCE LIMITED (DOING BUSINESS AS QUOTIENT)
  SUBSTANTIALLY EQUIVALENT 4
AMERICAN RED CROSS
  SUBSTANTIALLY EQUIVALENT 2
BIO-RAD MEDICAL DIAGNOSTICS GMBH
  SUBSTANTIALLY EQUIVALENT 3
DIAGAST
  SUBSTANTIALLY EQUIVALENT 2
HEMO BIOSCIENCE
  SUBSTANTIALLY EQUIVALENT 4
IMMUCOR, INC.
  SUBSTANTIALLY EQUIVALENT 2
MEDION GRIFOLS DIAGNOSTICS AG
  SUBSTANTIALLY EQUIVALENT 2
MICRO TYPING SYSTEMS INC.
  SUBSTANTIALLY EQUIVALENT 1
MILLIPORE (UK) LTD
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2015 4 4
2016 16 16
2017 19 19
2018 20 20
2019 10 10
2020 1 1
2022 1 1
2023 2 2
2024 2 2

Device Problems MDRs with this Device Problem Events in those MDRs
False Negative Result 61 61
False Positive Result 3 3
Off-Label Use 2 2
Nonstandard Device 2 2
Defective Device 2 2
Incorrect, Inadequate or Imprecise Result or Readings 2 2
Fluid/Blood Leak 1 1
Incorrect Or Inadequate Test Results 1 1
Insufficient Information 1 1
Short Fill 1 1
Human Factors Issue 1 1
Chemical Spillage 1 1
No Apparent Adverse Event 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Known Impact Or Consequence To Patient 36 36
No Consequences Or Impact To Patient 28 28
No Clinical Signs, Symptoms or Conditions 3 3
No Code Available 2 2
Chemical Exposure 2 2
Patient Problem/Medical Problem 1 1
No Information 1 1
Unspecified Eye / Vision Problem 1 1
Fever 1 1

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