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FDA 510(k)

BMC CATHETER CONNECTOR CABLE, MODEL RFP-101

K-Number: K023334 · 2002-12-31

ApplicantBaylis Medical Co., Inc.
Decision Date2002-12-31
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BMC CATHETER CONNECTOR CABLE, MODEL RFP-101 is the device name listed in this FDA 510(k) record. The listed applicant is Baylis Medical Co., Inc.. It received FDA 510(k) clearance on 2002-12-31 under 510(k) number K023334. 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 BMC CATHETER CONNECTOR CABLE, MODEL RFP-101?

BMC CATHETER CONNECTOR CABLE, MODEL RFP-101 is a medical device that received FDA 510(k) clearance on 2002-12-31. The listed applicant is Baylis Medical Co., Inc.. The 510(k) number is K023334.

When did BMC CATHETER CONNECTOR CABLE, MODEL RFP-101 receive FDA 510(k) clearance?

BMC CATHETER CONNECTOR CABLE, MODEL RFP-101 received FDA 510(k) clearance on 2002-12-31, under 510(k) number K023334.

Who is the listed applicant for BMC CATHETER CONNECTOR CABLE, MODEL RFP-101?

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

What is the FDA product code for BMC CATHETER CONNECTOR CABLE, MODEL RFP-101?

The FDA product code for BMC CATHETER CONNECTOR CABLE, MODEL RFP-101 is DSA.

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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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