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FDA 510(k)

ENDOSCOPE AND ACCESSORIES

K-Number: K926223 · 1993-04-20

ApplicantWeck Endoscopy
Decision Date1993-04-20
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Weck Endoscopy. It received FDA 510(k) clearance on 1993-04-20 under 510(k) number K926223. 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 ENDOSCOPE AND ACCESSORIES?

ENDOSCOPE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Weck Endoscopy. The 510(k) number is K926223.

When did ENDOSCOPE AND ACCESSORIES receive FDA 510(k) clearance?

ENDOSCOPE AND ACCESSORIES received FDA 510(k) clearance on 1993-04-20, under 510(k) number K926223.

Who is the listed applicant for ENDOSCOPE AND ACCESSORIES?

The FDA 510(k) record lists Weck Endoscopy as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSCOPE AND ACCESSORIES?

The FDA product code for ENDOSCOPE AND ACCESSORIES 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.

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Other records listing Weck Endoscopy 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.

K926203ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS)K930550ECO LIGATING CLIPK930082ENDOSCOPE AND ACCESSORIES

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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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