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FDA 510(k)

BARD STABILIZING CANNULA

K-Number: K930827 · 1993-05-14

Decision Date1993-05-14
Product CodeFAJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARD STABILIZING CANNULA 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 1993-05-14 under 510(k) number K930827. The device is classified under product code FAJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD STABILIZING CANNULA?

BARD STABILIZING CANNULA is a medical device that received FDA 510(k) clearance on 1993-05-14. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K930827.

When did BARD STABILIZING CANNULA receive FDA 510(k) clearance?

BARD STABILIZING CANNULA received FDA 510(k) clearance on 1993-05-14, under 510(k) number K930827.

Who is the listed applicant for BARD STABILIZING CANNULA?

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 STABILIZING CANNULA?

The FDA product code for BARD STABILIZING CANNULA is FAJ.

Related Clinical Trials

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.

Other records listing C.R. Bard, 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.

View all 616 devices →

Related Devices (Code: FAJ)

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.

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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