FDA 510(k)

SAUER ENDOSCOPE GUIDE AND INTUBATION AID

K-Number: K954125 · 1995-10-06

ApplicantKARL STORZ Endoscopy-America, Inc.

Decision Date1995-10-06

Product CodeEOQ

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

SAUER ENDOSCOPE GUIDE AND INTUBATION AID 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 1995-10-06 under 510(k) number K954125. 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 SAUER ENDOSCOPE GUIDE AND INTUBATION AID?

SAUER ENDOSCOPE GUIDE AND INTUBATION AID is a medical device that received FDA 510(k) clearance on 1995-10-06. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K954125.

When did SAUER ENDOSCOPE GUIDE AND INTUBATION AID receive FDA 510(k) clearance?

SAUER ENDOSCOPE GUIDE AND INTUBATION AID received FDA 510(k) clearance on 1995-10-06, under 510(k) number K954125.

Who is the listed applicant for SAUER ENDOSCOPE GUIDE AND INTUBATION AID?

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 SAUER ENDOSCOPE GUIDE AND INTUBATION AID?

The FDA product code for SAUER ENDOSCOPE GUIDE AND INTUBATION AID is EOQ.

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Other records listing KARL STORZ Endoscopy-America, Inc. as applicant

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Related Devices (Code: EOQ)

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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.