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FDA 510(k)

IMAGE1 GI CCU MODEL 22203020-114

K-Number: K111997 · 2012-04-06

Decision Date2012-04-06
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

IMAGE1 GI CCU MODEL 22203020-114 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 2012-04-06 under 510(k) number K111997. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMAGE1 GI CCU MODEL 22203020-114?

IMAGE1 GI CCU MODEL 22203020-114 is a medical device that received FDA 510(k) clearance on 2012-04-06. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K111997.

When did IMAGE1 GI CCU MODEL 22203020-114 receive FDA 510(k) clearance?

IMAGE1 GI CCU MODEL 22203020-114 received FDA 510(k) clearance on 2012-04-06, under 510(k) number K111997.

Who is the listed applicant for IMAGE1 GI CCU MODEL 22203020-114?

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 IMAGE1 GI CCU MODEL 22203020-114?

The FDA product code for IMAGE1 GI CCU MODEL 22203020-114 is FET.

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: FET)

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

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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