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FDA 510(k)

BARD ENDOSCOPIC INJECTION SYSTEM

K-Number: K933815 · 1993-12-01

ApplicantC.R. Bard, Inc.
Decision Date1993-12-01
Product CodeFBK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARD ENDOSCOPIC INJECTION SYSTEM 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 1993-12-01 under 510(k) number K933815. The device is classified under product code FBK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD ENDOSCOPIC INJECTION SYSTEM?

BARD ENDOSCOPIC INJECTION SYSTEM is a medical device that received FDA 510(k) clearance on 1993-12-01. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K933815.

When did BARD ENDOSCOPIC INJECTION SYSTEM receive FDA 510(k) clearance?

BARD ENDOSCOPIC INJECTION SYSTEM received FDA 510(k) clearance on 1993-12-01, under 510(k) number K933815.

Who is the listed applicant for BARD ENDOSCOPIC INJECTION SYSTEM?

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 ENDOSCOPIC INJECTION SYSTEM?

The FDA product code for BARD ENDOSCOPIC INJECTION SYSTEM is FBK.

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Related Devices (Code: FBK)

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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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