FDA 510(k)

CMOS VIDEO RHINO-LARYNGOSCOPE SYSTEM MODEL 11101CM

K-Number: K103467 · 2012-06-28

ApplicantKARL STORZ Endoscopy-America, Inc.

Decision Date2012-06-28

Product CodeEOB

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

CMOS VIDEO RHINO-LARYNGOSCOPE SYSTEM MODEL 11101CM 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 2012-06-28 under 510(k) number K103467. 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 CMOS VIDEO RHINO-LARYNGOSCOPE SYSTEM MODEL 11101CM?

CMOS VIDEO RHINO-LARYNGOSCOPE SYSTEM MODEL 11101CM is a medical device that received FDA 510(k) clearance on 2012-06-28. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K103467.

When did CMOS VIDEO RHINO-LARYNGOSCOPE SYSTEM MODEL 11101CM receive FDA 510(k) clearance?

CMOS VIDEO RHINO-LARYNGOSCOPE SYSTEM MODEL 11101CM received FDA 510(k) clearance on 2012-06-28, under 510(k) number K103467.

Who is the listed applicant for CMOS VIDEO RHINO-LARYNGOSCOPE SYSTEM MODEL 11101CM?

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 CMOS VIDEO RHINO-LARYNGOSCOPE SYSTEM MODEL 11101CM?

The FDA product code for CMOS VIDEO RHINO-LARYNGOSCOPE SYSTEM MODEL 11101CM is EOB.

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

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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.