Neoserv 824
FDA 510(k) K900729 · Burdick Corp.
510(k) numberK900729
Submission
- Device name
- Neoserv 824
- Applicant
- Burdick Corp.
Miltoon, WI, US - Received
- February 15, 1990
- Decision date
- June 8, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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| K943959 | Eclipse 4 ElectrocardiographLOS · Traditional | 05/17/1995SE |
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| K942438 | Altair 6100 Cassette RecorderDSH · Traditional | 08/05/1994SE |
| K904032 | Elite II ElectrocardiographLOS · Traditional | 07/24/1991SE |
| K903565 | E560 ElectrocardiographLOS · Traditional | 07/24/1991SE |
Questions and answers
When was Neoserv 824 cleared by the FDA?
Neoserv 824 (K900729) received a 510(k) decision of Substantially Equivalent on June 8, 1990, 113 days after the submission was received.