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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 the device name listed in this FDA 510(k) record. The listed applicant is Baylis Medical Technologies, Inc.. It received FDA 510(k) clearance on 2023-05-30 under 510(k) 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. The listed applicant is Baylis Medical Technologies, Inc.. The 510(k) number is K230571.

When did RFP-100A Connector Cable (Single Use) receive FDA 510(k) clearance?

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

Who is the listed applicant for RFP-100A Connector Cable (Single Use)?

The FDA 510(k) record lists Baylis Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

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Other records listing Baylis Medical Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254114Baylis Connector CableK250275PrecisePath™ Radiofrequency Puncture Generator and PrecisePath™ FootswitchK251158PowerWire® 14 Radiofrequency Guidewire KitK232562PowerWire Radiofrequency Guidewire Kit

Related Devices (Code: DSA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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

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