Alexander Manufacturing Co. Rechargeable Battery Part Number M12/500
FDA 510(k) K971826 · Alexander Mfg. Co.
510(k) numberK971826
Submission
- Device name
- Alexander Manufacturing Co. Rechargeable Battery Part Number M12/500
- Applicant
- Alexander Mfg. Co.
Mason City, IA, US - Received
- May 16, 1997
- Decision date
- July 3, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- LDR – Controller, Infusion, Intravascular, Electronic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5725
- Specialty
- General Hospital
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| K232316 | DEKA Infusion System, DEKA Administration SetLDR · Traditional | Deka Research and Development | 03/01/2024SE |
| K153760 | Volumetric Infusion ControllerLDR · Traditional | DEKA Research & Development | 10/03/2016SE |
| K963136 | Pacer Model 100 Infusion ControllerLDR · Traditional | Health Watch, Inc. | 10/10/1997SE |
| K971865 | Alexander Manufacturing Co. Rechargeable Battery Part Number M12/500-3PLDR · Traditional | Alexander Mfg. Co. | 07/03/1997SE |
| K934543 | Universal Controller, Model 100LDR · Traditional | Metamed, Inc. | 03/29/1994SE |
| K935236 | Flow Controlling Extension SetLDR · Traditional | Block Medical, Inc. | 02/24/1994SE |
| K905498 | Stat 2 IV PumpetteLDR · Traditional | The Master Medical Corp. | 04/16/1991SE |
| K905497 | Master Flow I.V. PumpetteLDR · Traditional | The Master Medical Corp. | 04/16/1991SE |
| K896907 | 3M IV Flow RegulatorLDR · Traditional | 3M Company | 02/26/1990SE |
More from 3M Company
| 510(k) | Device | Decision |
|---|---|---|
| K982896 | Alexander Manufacturing Co. Rechargeable Battery Part Number LP9LDD · Traditional | 10/21/1998ST |
| K981776 | Alexander Manufacturing Co. Battery Part Number MC146XFRN · Traditional | 08/03/1998SE |
| K981728 | Alexander Manufacturing Co. Battery Part Number H134BZQ · Traditional | 06/26/1998ST |
| K980224 | Alexander Manufacturing Co. Rechargeable Battery Part Number MS822MOQ · Traditional | 04/02/1998SE |
| K974061 | Rechargeable Battery Part Number GL825-200DXN · Traditional | 01/16/1998SE |
| K973851 | Alexander Manufacturing Co. Rechargeable Battery #M12/630FRN · Traditional | 01/05/1998SE |
| K973850 | Alexander Manufacturing Co. Rechargeable Battery #M007HFO · Traditional | 11/12/1997SE |
| K972746 | Alexander Manufacturing Co. Rechargeable Battery Part Number LP6/100DPS · Traditional | 10/21/1997SE |
| K972780 | Alexander Manufacturing Co. Rechargeable Battery Part Number GL625MRZ · Traditional | 10/20/1997SE |
| K972779 | Alexander Manufacturing Co. Rechargeable Battery Part Number MS3030-PMRZ · Traditional | 10/20/1997SE |
Questions and answers
When was Alexander Manufacturing Co. Rechargeable Battery Part Number M12/500 cleared by the FDA?
Alexander Manufacturing Co. Rechargeable Battery Part Number M12/500 (K971826) received a 510(k) decision of Substantially Equivalent on July 3, 1997, 48 days after the submission was received.
What is the product code of K971826?
The FDA product code is LDR – Controller, Infusion, Intravascular, Electronic, a Class II (moderate risk) device regulated under 21 CFR 880.5725.