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FDA 510(k)

DISPOSABLE ENDOSCOPIC RETRIEVAL DEVICE

K-Number: K962676 · 1996-10-04

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1996-10-04
Product CodeFGO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE ENDOSCOPIC RETRIEVAL DEVICE 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 1996-10-04 under 510(k) number K962676. The device is classified under product code FGO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE ENDOSCOPIC RETRIEVAL DEVICE?

DISPOSABLE ENDOSCOPIC RETRIEVAL DEVICE is a medical device that received FDA 510(k) clearance on 1996-10-04. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K962676.

When did DISPOSABLE ENDOSCOPIC RETRIEVAL DEVICE receive FDA 510(k) clearance?

DISPOSABLE ENDOSCOPIC RETRIEVAL DEVICE received FDA 510(k) clearance on 1996-10-04, under 510(k) number K962676.

Who is the listed applicant for DISPOSABLE ENDOSCOPIC RETRIEVAL DEVICE?

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 DISPOSABLE ENDOSCOPIC RETRIEVAL DEVICE?

The FDA product code for DISPOSABLE ENDOSCOPIC RETRIEVAL DEVICE is FGO.

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Related Devices (Code: FGO)

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.

K001563SCIPRO(TM) FLEXIBLE STONE DISLODGER AND RETRIEVAL SETScion Cardiovascular, Inc.K970121STONE DISLODGER, BASKETBoston Scientific CorpK963750RETRIEVAL SNAREBoston Scientific CorpK951309STONE DISLODGER, BASKETBoston Scientific CorpK933261GRASPING FORCEPSSurgitekK934598GRASPING FORCEPS OR RETRIEVAL FORCEPSAnnex Medical, Inc.

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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