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FDA 510(k)

ENDOPATH SURESEAL REDUCER CAP

K-Number: K001220 · 2000-05-16

ApplicantEthicon Endo-Surgery, Inc.
Decision Date2000-05-16
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENDOPATH SURESEAL REDUCER CAP 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 2000-05-16 under 510(k) number K001220. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOPATH SURESEAL REDUCER CAP?

ENDOPATH SURESEAL REDUCER CAP is a medical device that received FDA 510(k) clearance on 2000-05-16. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K001220.

When did ENDOPATH SURESEAL REDUCER CAP receive FDA 510(k) clearance?

ENDOPATH SURESEAL REDUCER CAP received FDA 510(k) clearance on 2000-05-16, under 510(k) number K001220.

Who is the listed applicant for ENDOPATH SURESEAL REDUCER CAP?

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 ENDOPATH SURESEAL REDUCER CAP?

The FDA product code for ENDOPATH SURESEAL REDUCER CAP is HET.

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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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