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FDA 510(k)

WGL ENDOSCOPIC GRASPER W/DETACHABLE STRAP

K-Number: K954649 · 1995-12-22

Decision Date1995-12-22
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WGL ENDOSCOPIC GRASPER W/DETACHABLE STRAP 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 1995-12-22 under 510(k) number K954649. 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 W/DETACHABLE STRAP?

WGL ENDOSCOPIC GRASPER W/DETACHABLE STRAP is a medical device that received FDA 510(k) clearance on 1995-12-22. The listed applicant is Wilson Greatbatch Technologies, Inc.. The 510(k) number is K954649.

When did WGL ENDOSCOPIC GRASPER W/DETACHABLE STRAP receive FDA 510(k) clearance?

WGL ENDOSCOPIC GRASPER W/DETACHABLE STRAP received FDA 510(k) clearance on 1995-12-22, under 510(k) number K954649.

Who is the listed applicant for WGL ENDOSCOPIC GRASPER W/DETACHABLE STRAP?

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 W/DETACHABLE STRAP?

The FDA product code for WGL ENDOSCOPIC GRASPER W/DETACHABLE STRAP is GCJ.

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 Wilson Greatbatch Technologies, 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 9 devices →

Related Devices (Code: GCJ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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