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FDA 510(k)

KARL STORZ RIGID TELESCOPES FOR ENT ENDOSCOPIC PROCEDURES

K-Number: K945788 · 1995-01-25

ApplicantKARL STORZ Endoscopy-America, Inc.
Decision Date1995-01-25
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

KARL STORZ RIGID TELESCOPES FOR ENT ENDOSCOPIC PROCEDURES is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1995-01-25 under 510(k) number K945788. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ RIGID TELESCOPES FOR ENT ENDOSCOPIC PROCEDURES?

KARL STORZ RIGID TELESCOPES FOR ENT ENDOSCOPIC PROCEDURES is a medical device that received FDA 510(k) clearance on 1995-01-25. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K945788.

When did KARL STORZ RIGID TELESCOPES FOR ENT ENDOSCOPIC PROCEDURES receive FDA 510(k) clearance?

KARL STORZ RIGID TELESCOPES FOR ENT ENDOSCOPIC PROCEDURES received FDA 510(k) clearance on 1995-01-25, under 510(k) number K945788.

Who is the listed applicant for KARL STORZ RIGID TELESCOPES FOR ENT ENDOSCOPIC PROCEDURES?

The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KARL STORZ RIGID TELESCOPES FOR ENT ENDOSCOPIC PROCEDURES?

The FDA product code for KARL STORZ RIGID TELESCOPES FOR ENT ENDOSCOPIC PROCEDURES is EOB.

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Other records listing KARL STORZ Endoscopy-America, 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.

K252624KARL STORZ Laryngoscopes and AccessoriesK240506KARL STORZ HoldersK223885HOPKINS TelescopesK230359KOH Ultramicro Injection Cannula (26167NN); Suction a. Irrig. Cannula,L. 36cm (37360CP); Suction a. Irrig. Cannula,L. 36cm (37360SC); Suction and Irrig Cannula,l. 36cm (37560LH); Suction a. Irrig. Cannula,L. 30cm (37260LH); KOH Ultramicro Injection Needle (26167NA); Puncture Needle, LUER-lock (26178R); Suction a. Irrig. Cannula,L. 43cm (37460LH); Suction a. Irrig. Cannula,L. 36cm (37360LH); Puncture Needle, dia. 1.6 mm, 36 cm (26175R); Two-Way Stopcock (26167H); Injection Needle, LUER-K223520UNIDRIVE SIII SystemK223923HOPKINS Telescopes

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Related Devices (Code: EOB)

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K254299CLEARVISION Irrigation Sheath 0° (7241AS); CLEARVISION Irrigation Sheath 30° (7241BS); CLEARVISION Irrigation Sheath 45° (7241FS)Karl Storz SE & CO. KGK261544Hydro Irrigation SystemStryker InstrumentsK254133ENTity USB Videoscope SystemOptim, LLCK253184Video Rhinolaryngoscope System (Disposable Video Rhinolaryngoscope SP11A Endoscopic Video Processor M110B)Zhuhai Wesee Meditech Co., Ltd.K252050Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241DOlympus Medical Systems CorporationK241731Outlook Surgical Versa One System (8900139)Resnent, LLC

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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