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FDA 510(k)

RFP-100A Connector Cable (Single Use)

K-Number: K230571 · 2023-05-30

ApplicantBaylis Medical Technologies, Inc.
Decision Date2023-05-30
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RFP-100A Connector Cable (Single Use) is a medical device manufactured by Baylis Medical Technologies, Inc.. It received FDA 510(k) clearance on 2023-05-30 under approval number K230571. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RFP-100A Connector Cable (Single Use)?

RFP-100A Connector Cable (Single Use) is a medical device that received FDA 510(k) clearance on 2023-05-30. It is manufactured by Baylis Medical Technologies, Inc.. The 510(k) number is K230571.

When was RFP-100A Connector Cable (Single Use) approved by the FDA?

RFP-100A Connector Cable (Single Use) received FDA 510(k) clearance on 2023-05-30, under approval number K230571.

What company makes RFP-100A Connector Cable (Single Use)?

RFP-100A Connector Cable (Single Use) is manufactured by Baylis Medical Technologies, Inc..

What is the FDA product code for RFP-100A Connector Cable (Single Use)?

The FDA product code for RFP-100A Connector Cable (Single Use) is DSA.

Other Devices by Baylis Medical Technologies, Inc.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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