Harmony Inr Monitoring System
FDA 510(k) K022922 · Lifescan, Inc.
510(k) numberK022922
Submission
- Device name
- Harmony Inr Monitoring System
- Applicant
- Lifescan, Inc.
Milpitas, CA, US - Received
- September 4, 2002
- Decision date
- September 30, 2002
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- GJS – Test, Time, Prothrombin
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 864.7750
- Specialty
- Hematology
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| K231711 | microINR SystemGJS · Special | Iline Microsystems, S.L. | 07/11/2023SE |
| K211485 | STA- NeoPTimalGJS · Traditional | Diagnostica Stago S.A.S | 12/23/2022SE |
| K212779 | Coag-Sense Prothrombin (PT) / INR Monitoring System for Patient Self-TestingGJS · Special | Coagusense, Inc. | 10/05/2022SE |
| K213426 | HemosIL ReadiPlasTinGJS · Traditional | Instrumentation Laboratory CO | 08/16/2022SE |
| K201185 | microINR SystemGJS · Traditional | Iline Microsystems, S.L. | 12/18/2020SE |
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Questions and answers
When was Harmony Inr Monitoring System cleared by the FDA?
Harmony Inr Monitoring System (K022922) received a 510(k) decision of Substantially Equivalent on September 30, 2002, 26 days after the submission was received.
What is the product code of K022922?
The FDA product code is GJS – Test, Time, Prothrombin, a Class II (moderate risk) device regulated under 21 CFR 864.7750.