FDA 510(k)

ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLER

K-Number: K102632 · 2010-10-07

Decision Date2010-10-07

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLER 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 2010-10-07 under 510(k) number K102632. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLER?

ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLER is a medical device that received FDA 510(k) clearance on 2010-10-07. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K102632.

When did ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLER receive FDA 510(k) clearance?

ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLER received FDA 510(k) clearance on 2010-10-07, under 510(k) number K102632.

Who is the listed applicant for ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLER?

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 ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLER?

The FDA product code for ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLER is GDW.

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Other records listing Ethicon Endo-Surgery, 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.