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FDA 510(k)

WGL ENDOSCOPIC GRASPER*

K-Number: K950063 · 1995-01-27

ApplicantWilson Greatbatch Technologies, Inc.
Decision Date1995-01-27
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WGL ENDOSCOPIC GRASPER* is the device name listed in this FDA 510(k) record. The listed applicant is Wilson Greatbatch Technologies, Inc.. It received FDA 510(k) clearance on 1995-01-27 under 510(k) number K950063. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WGL ENDOSCOPIC GRASPER*?

WGL ENDOSCOPIC GRASPER* is a medical device that received FDA 510(k) clearance on 1995-01-27. The listed applicant is Wilson Greatbatch Technologies, Inc.. The 510(k) number is K950063.

When did WGL ENDOSCOPIC GRASPER* receive FDA 510(k) clearance?

WGL ENDOSCOPIC GRASPER* received FDA 510(k) clearance on 1995-01-27, under 510(k) number K950063.

Who is the listed applicant for WGL ENDOSCOPIC GRASPER*?

The FDA 510(k) record lists Wilson Greatbatch Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WGL ENDOSCOPIC GRASPER*?

The FDA product code for WGL ENDOSCOPIC GRASPER* is GCJ.

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Other records listing Wilson Greatbatch Technologies, Inc. as applicant

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Related Devices (Code: GCJ)

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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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