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FDA 510(k)

SCHOELLY RIGID ENDOSCOPES

K-Number: K992437 · 1999-09-14

ApplicantFiber Imaging Technologies, Inc.
Decision Date1999-09-14
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SCHOELLY RIGID ENDOSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is Fiber Imaging Technologies, Inc.. It received FDA 510(k) clearance on 1999-09-14 under 510(k) number K992437. 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 SCHOELLY RIGID ENDOSCOPES?

SCHOELLY RIGID ENDOSCOPES is a medical device that received FDA 510(k) clearance on 1999-09-14. The listed applicant is Fiber Imaging Technologies, Inc.. The 510(k) number is K992437.

When did SCHOELLY RIGID ENDOSCOPES receive FDA 510(k) clearance?

SCHOELLY RIGID ENDOSCOPES received FDA 510(k) clearance on 1999-09-14, under 510(k) number K992437.

Who is the listed applicant for SCHOELLY RIGID ENDOSCOPES?

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

What is the FDA product code for SCHOELLY RIGID ENDOSCOPES?

The FDA product code for SCHOELLY RIGID ENDOSCOPES 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 Fiber Imaging 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.

K993300COLDLIGHTSOURCE PL3000K992527URETERO-RENOSCOPEK992040FLEXISCOPE II ARTHROSCOPES AND ACCESSORIESK991560NASO-LARYNGO-PHARYNGOSCOPE

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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