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FDA 510(k)

INSCOPE MULTI-CLIP APPLIER, MODELS IN22321, IN23321

K-Number: K051950 · 2005-10-07

ApplicantEthicon Endo-Surgery, Inc.
Decision Date2005-10-07
Product CodeMND
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INSCOPE MULTI-CLIP APPLIER, MODELS IN22321, IN23321 is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, Inc.. It received FDA 510(k) clearance on 2005-10-07 under 510(k) number K051950. The device is classified under product code MND. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSCOPE MULTI-CLIP APPLIER, MODELS IN22321, IN23321?

INSCOPE MULTI-CLIP APPLIER, MODELS IN22321, IN23321 is a medical device that received FDA 510(k) clearance on 2005-10-07. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K051950.

When did INSCOPE MULTI-CLIP APPLIER, MODELS IN22321, IN23321 receive FDA 510(k) clearance?

INSCOPE MULTI-CLIP APPLIER, MODELS IN22321, IN23321 received FDA 510(k) clearance on 2005-10-07, under 510(k) number K051950.

Who is the listed applicant for INSCOPE MULTI-CLIP APPLIER, MODELS IN22321, IN23321?

The FDA 510(k) record lists Ethicon Endo-Surgery, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSCOPE MULTI-CLIP APPLIER, MODELS IN22321, IN23321?

The FDA product code for INSCOPE MULTI-CLIP APPLIER, MODELS IN22321, IN23321 is MND.

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Other records listing Ethicon Endo-Surgery, Inc. as applicant

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Related Devices (Code: MND)

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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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