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FDA 510(k)

BARD ULTRAVIEW MULTIPLE BAND LIGATOR, MODEL 00700U

K-Number: K033245 · 2003-11-06

ApplicantC.R. Bard, Inc.
Decision Date2003-11-06
Product CodeMND
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARD ULTRAVIEW MULTIPLE BAND LIGATOR, MODEL 00700U is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2003-11-06 under 510(k) number K033245. The device is classified under product code MND. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD ULTRAVIEW MULTIPLE BAND LIGATOR, MODEL 00700U?

BARD ULTRAVIEW MULTIPLE BAND LIGATOR, MODEL 00700U is a medical device that received FDA 510(k) clearance on 2003-11-06. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K033245.

When did BARD ULTRAVIEW MULTIPLE BAND LIGATOR, MODEL 00700U receive FDA 510(k) clearance?

BARD ULTRAVIEW MULTIPLE BAND LIGATOR, MODEL 00700U received FDA 510(k) clearance on 2003-11-06, under 510(k) number K033245.

Who is the listed applicant for BARD ULTRAVIEW MULTIPLE BAND LIGATOR, MODEL 00700U?

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

What is the FDA product code for BARD ULTRAVIEW MULTIPLE BAND LIGATOR, MODEL 00700U?

The FDA product code for BARD ULTRAVIEW MULTIPLE BAND LIGATOR, MODEL 00700U is MND.

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Related Devices (Code: MND)

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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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