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FDA 510(k)

KARL STORZ BRONCHOSCOPE ACCESSORIES

K-Number: K943700 · 1994-08-23

Decision Date1994-08-23
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

KARL STORZ BRONCHOSCOPE ACCESSORIES 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 1994-08-23 under 510(k) number K943700. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ BRONCHOSCOPE ACCESSORIES?

KARL STORZ BRONCHOSCOPE ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-08-23. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K943700.

When did KARL STORZ BRONCHOSCOPE ACCESSORIES receive FDA 510(k) clearance?

KARL STORZ BRONCHOSCOPE ACCESSORIES received FDA 510(k) clearance on 1994-08-23, under 510(k) number K943700.

Who is the listed applicant for KARL STORZ BRONCHOSCOPE ACCESSORIES?

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 BRONCHOSCOPE ACCESSORIES?

The FDA product code for KARL STORZ BRONCHOSCOPE ACCESSORIES is EOQ.

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.

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.

View all 355 devices →

Related Devices (Code: EOQ)

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.

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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