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FDA 510(k)

DAVOL GAUDERER-PONSKY PERCUTAN-ENDOSCOP

K-Number: K843305 · 1984-10-11

ApplicantC.R. Bard, Inc.
Decision Date1984-10-11
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAVOL GAUDERER-PONSKY PERCUTAN-ENDOSCOP 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 1984-10-11 under 510(k) number K843305. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVOL GAUDERER-PONSKY PERCUTAN-ENDOSCOP?

DAVOL GAUDERER-PONSKY PERCUTAN-ENDOSCOP is a medical device that received FDA 510(k) clearance on 1984-10-11. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K843305.

When did DAVOL GAUDERER-PONSKY PERCUTAN-ENDOSCOP receive FDA 510(k) clearance?

DAVOL GAUDERER-PONSKY PERCUTAN-ENDOSCOP received FDA 510(k) clearance on 1984-10-11, under 510(k) number K843305.

Who is the listed applicant for DAVOL GAUDERER-PONSKY PERCUTAN-ENDOSCOP?

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 DAVOL GAUDERER-PONSKY PERCUTAN-ENDOSCOP?

The FDA product code for DAVOL GAUDERER-PONSKY PERCUTAN-ENDOSCOP is KNT.

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Related Devices (Code: KNT)

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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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