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FDA 510(k)

KARL STORZ TRANS-NASAL ESOPHAGOSCOPE

K-Number: K051972 · 2005-08-15

ApplicantKARL STORZ Endoscopy-America, Inc.
Decision Date2005-08-15
Product CodeEOX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

KARL STORZ TRANS-NASAL ESOPHAGOSCOPE 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 2005-08-15 under 510(k) number K051972. The device is classified under product code EOX. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ TRANS-NASAL ESOPHAGOSCOPE?

KARL STORZ TRANS-NASAL ESOPHAGOSCOPE is a medical device that received FDA 510(k) clearance on 2005-08-15. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K051972.

When did KARL STORZ TRANS-NASAL ESOPHAGOSCOPE receive FDA 510(k) clearance?

KARL STORZ TRANS-NASAL ESOPHAGOSCOPE received FDA 510(k) clearance on 2005-08-15, under 510(k) number K051972.

Who is the listed applicant for KARL STORZ TRANS-NASAL ESOPHAGOSCOPE?

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 TRANS-NASAL ESOPHAGOSCOPE?

The FDA product code for KARL STORZ TRANS-NASAL ESOPHAGOSCOPE is EOX.

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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: EOX)

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.

K233142EndoSign® Cell collection device (ES-CYT-102)Cyted LimitedK230339EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.K223072PENTAX Medical Video Esophagoscope EE17-J10Pentax of America, Inc.K222366EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.K203450EsophaCap Swallowable Cellular Retrieval Device (changed from Cell-Mata)Capnostics, LLCK210137EsoCheck Cell Collection DeviceLucid Diagnostics, 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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