Filter, Eyrpur Disposable Leukocite
FDA 510(k) K781803 · Metrix Teknika, Inc.
510(k) numberK781803
Submission
- Device name
- Filter, Eyrpur Disposable Leukocite
- Applicant
- Metrix Teknika, Inc.
- Received
- October 23, 1978
- Decision date
- January 17, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- GKT – Separator, Automated, Blood Cell, Diagnostic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 864.9245
- Specialty
- Hematology
Other 510(k)s with product code GKT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K200530 | AMICUS Separator SystemGKT · Traditional | Fresenius Kabi AG | 09/11/2020SE |
| K162462 | AMICUS Separator System, AMICUS Separator System; RefurbishedGKT · Traditional | Fresenius Kabi USA,Llc | 11/23/2016SE |
| K822521 | Automated Blood Cell SeparatorGKT · Traditional | Cryosan, Inc. | 09/30/1982SE |
| K820396 | Automated Blood Cell Separ. Disp. SftwrGKT · Traditional | Pheragen Technology Corp. | 04/27/1982SE |
| K801233 | Celltrifuge IIGKT · Traditional | Travenol Laboratories, S.A. | 10/31/1980SE |
| K791106 | Sterile, Disposable Centrifuge BowlGKT · Traditional | Travenol Laboratories, S.A. | 08/10/1979SE |
| K790105 | Terumo ImugardGKT · Traditional | Terumo America, Inc. | 05/24/1979SE |
| K771258 | Blood Cell Separator 2997GKT · Traditional | Intl. Business Machines | 09/06/1977SE |
| K760856 | Blood Cell Processor Model 2 IBM 2991GKT · Traditional | Intl. Business Machines | 01/10/1977SE |
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Questions and answers
When was Filter, Eyrpur Disposable Leukocite cleared by the FDA?
Filter, Eyrpur Disposable Leukocite (K781803) received a 510(k) decision of Substantially Equivalent on January 17, 1979, 86 days after the submission was received.
What is the product code of K781803?
The FDA product code is GKT – Separator, Automated, Blood Cell, Diagnostic, a Class II (moderate risk) device regulated under 21 CFR 864.9245.