Siemens Medical Infromation Bus (Mib II) Protocol Converter
FDA 510(k) K020277 · Siemens Medical Solutions USA, Inc.
510(k) numberK020277
Submission
- Device name
- Siemens Medical Infromation Bus (Mib II) Protocol Converter
- Applicant
- Siemens Medical Solutions USA, Inc.
Danvers, MA, US - Received
- January 28, 2002
- Decision date
- February 19, 2002
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DRQ – Amplifier And Signal Conditioner, Transducer Signal
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2060
- Specialty
- Cardiovascular
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Questions and answers
When was Siemens Medical Infromation Bus (Mib II) Protocol Converter cleared by the FDA?
Siemens Medical Infromation Bus (Mib II) Protocol Converter (K020277) received a 510(k) decision of Substantially Equivalent on February 19, 2002, 22 days after the submission was received.
What is the product code of K020277?
The FDA product code is DRQ – Amplifier And Signal Conditioner, Transducer Signal, a Class II (moderate risk) device regulated under 21 CFR 870.2060.