Acta Metra/Acta Gnosis Firmware Package
FDA 510(k) K900385 · Parexel Intl. Corp.
510(k) numberK900385
Submission
- Device name
- Acta Metra/Acta Gnosis Firmware Package
- Applicant
- Parexel Intl. Corp.
Cambridge, MS, US - Received
- January 29, 1990
- Decision date
- July 9, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DSI – Detector And Alarm, Arrhythmia
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1025
- Specialty
- Cardiovascular
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|---|---|---|---|
| K243349 | BodyGuardian Remote Monitoring System (BGRMS v3.0)DSI · Traditional | Boston Scientific Cardiac Diagnostic… | 01/23/2026SE |
| K250356 | MoMe ARC® Wireless Ambulatory ECG Monitoring and Detection System (32000)DSI · Traditional | Infobionic, Inc. | 07/29/2025SE |
| K240177 | Zio AT® device (A100A1001)DSI · Traditional | iRhythm Technologies, Inc. | 10/30/2024SE |
| K230265 | MoMe® ARC Wireless Ambulatory ECG Monitoring and Detection SystemDSI · Abbreviated | Infobionic, Inc. | 10/06/2023SE |
| K231276 | SmartCardia 7L PlatformDSI · Traditional | Smartcardia SA | 08/30/2023SE |
| K193104 | Unified Arrhythmia Diagnostic System PocketECG IVDSI · Special | Medicalgorithmics S.A. | 04/09/2020SE |
| K192732 | BodyGuardian Remote Monitoring SystemDSI · Traditional | Preventice Technologies, Inc. | 03/26/2020SE |
| K190574 | Patient Assistant Model PA97000DSI · Traditional | Medtronic, Inc. | 09/24/2019SE |
| K182532 | Liba3 SystemDSI · Traditional | National Cardiac, Inc. | 05/15/2019SE |
| K181658 | MobileECG 2 BTDSI · Traditional | Memtec Corporation | 03/26/2019SE |
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| K864519 | Philips Computed Radiography System (PCR)LLZ · Traditional | 02/13/1987SE |
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| K862415 | Type 633 Computed Radiography (CR) FilmIWZ · Traditional | 07/01/1986SE |
| K853295 | Emodren Exchangeable Plastic BellowsGCY · Traditional | 08/20/1985SE |
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Questions and answers
When was Acta Metra/Acta Gnosis Firmware Package cleared by the FDA?
Acta Metra/Acta Gnosis Firmware Package (K900385) received a 510(k) decision of Substantially Equivalent on July 9, 1991, 526 days after the submission was received.
What is the product code of K900385?
The FDA product code is DSI – Detector And Alarm, Arrhythmia, a Class II (moderate risk) device regulated under 21 CFR 870.1025.