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FDA 510(k)

REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS

K-Number: K070859 · 2007-09-12

ApplicantSterilmed, Inc.
Decision Date2007-09-12
Product CodeNLL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2007-09-12 under 510(k) number K070859. The device is classified under product code NLL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS?

REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS is a medical device that received FDA 510(k) clearance on 2007-09-12. The listed applicant is Sterilmed, Inc.. The 510(k) number is K070859.

When did REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS receive FDA 510(k) clearance?

REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS received FDA 510(k) clearance on 2007-09-12, under 510(k) number K070859.

Who is the listed applicant for REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS?

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

What is the FDA product code for REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS?

The FDA product code for REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS is NLL.

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Related Devices (Code: NLL)

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.

K070930REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERSSterilmed, Inc.K033578REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERSClearmedical, Inc.

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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