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FDA 510(k)

KARL STORZ TWIN TRANSILLUMINATOR

K-Number: K962032 · 1996-07-05

ApplicantKARL STORZ Endoscopy-America, Inc.
Decision Date1996-07-05
Product CodeMQW
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

KARL STORZ TWIN TRANSILLUMINATOR 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 1996-07-05 under 510(k) number K962032. The device is classified under product code MQW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ TWIN TRANSILLUMINATOR?

KARL STORZ TWIN TRANSILLUMINATOR is a medical device that received FDA 510(k) clearance on 1996-07-05. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K962032.

When did KARL STORZ TWIN TRANSILLUMINATOR receive FDA 510(k) clearance?

KARL STORZ TWIN TRANSILLUMINATOR received FDA 510(k) clearance on 1996-07-05, under 510(k) number K962032.

Who is the listed applicant for KARL STORZ TWIN TRANSILLUMINATOR?

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 TWIN TRANSILLUMINATOR?

The FDA product code for KARL STORZ TWIN TRANSILLUMINATOR is MQW.

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 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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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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