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FDA 510(k)

BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755

K-Number: K003570 · 2001-06-06

ApplicantBacchus Vascular, Inc.
Decision Date2001-06-06
Product CodeMCW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755 is the device name listed in this FDA 510(k) record. The listed applicant is Bacchus Vascular, Inc.. It received FDA 510(k) clearance on 2001-06-06 under 510(k) number K003570. The device is classified under product code MCW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755?

BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755 is a medical device that received FDA 510(k) clearance on 2001-06-06. The listed applicant is Bacchus Vascular, Inc.. The 510(k) number is K003570.

When did BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755 receive FDA 510(k) clearance?

BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755 received FDA 510(k) clearance on 2001-06-06, under 510(k) number K003570.

Who is the listed applicant for BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755?

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

What is the FDA product code for BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755?

The FDA product code for BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755 is MCW.

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Other records listing Bacchus Vascular, 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.

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Related Devices (Code: MCW)

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

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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