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FDA 510(k)

LAPAROSCOPIC VESSEL ARTICULATOR

K-Number: K911475 · 1991-07-02

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1991-07-02
Product CodeDWP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC VESSEL ARTICULATOR is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1991-07-02 under 510(k) number K911475. The device is classified under product code DWP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPAROSCOPIC VESSEL ARTICULATOR?

LAPAROSCOPIC VESSEL ARTICULATOR is a medical device that received FDA 510(k) clearance on 1991-07-02. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K911475.

When did LAPAROSCOPIC VESSEL ARTICULATOR receive FDA 510(k) clearance?

LAPAROSCOPIC VESSEL ARTICULATOR received FDA 510(k) clearance on 1991-07-02, under 510(k) number K911475.

Who is the listed applicant for LAPAROSCOPIC VESSEL ARTICULATOR?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROSCOPIC VESSEL ARTICULATOR?

The FDA product code for LAPAROSCOPIC VESSEL ARTICULATOR is DWP.

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Related Devices (Code: DWP)

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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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