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FDA 510(k)

ENDOPATH RELOADABLE LINEAR CUTTER

K-Number: K930934 · 1994-03-11

ApplicantETHICON, Inc.
Decision Date1994-03-11
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENDOPATH RELOADABLE LINEAR CUTTER is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1994-03-11 under 510(k) number K930934. 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 RELOADABLE LINEAR CUTTER?

ENDOPATH RELOADABLE LINEAR CUTTER is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is ETHICON, Inc.. The 510(k) number is K930934.

When did ENDOPATH RELOADABLE LINEAR CUTTER receive FDA 510(k) clearance?

ENDOPATH RELOADABLE LINEAR CUTTER received FDA 510(k) clearance on 1994-03-11, under 510(k) number K930934.

Who is the listed applicant for ENDOPATH RELOADABLE LINEAR CUTTER?

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

What is the FDA product code for ENDOPATH RELOADABLE LINEAR CUTTER?

The FDA product code for ENDOPATH RELOADABLE LINEAR CUTTER 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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