RF Choke Cable
FDA 510(k) K771750 · C.R. Bard, Inc.
510(k) numberK771750
Submission
- Device name
- RF Choke Cable
- Applicant
- C.R. Bard, Inc.
Mchenry, IL, US - Received
- September 15, 1977
- Decision date
- September 30, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DSA – Cable, Transducer And Electrode, Patient, (Including Connector)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2900
- Specialty
- Cardiovascular
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| K222712 | Fogg System Patient Monitoring CablesDSA · Traditional | Fogg System Company, Inc. | 11/22/2023SE |
| K230571 | RFP-100A Connector Cable (Single Use)DSA · Traditional | Baylis Medical Technologies, Inc. | 05/30/2023SE |
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Questions and answers
When was RF Choke Cable cleared by the FDA?
RF Choke Cable (K771750) received a 510(k) decision of Substantially Equivalent on September 30, 1977, 15 days after the submission was received.
What is the product code of K771750?
The FDA product code is DSA – Cable, Transducer And Electrode, Patient, (Including Connector), a Class II (moderate risk) device regulated under 21 CFR 870.2900.