FDA 510(k)

REPROCESSED ENDOSCOPIC TROCAR

K-Number: K052299 · 2006-05-23

Decision Date2006-05-23

Product CodeNLM

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

REPROCESSED ENDOSCOPIC TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2006-05-23 under 510(k) number K052299. The device is classified under product code NLM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED ENDOSCOPIC TROCAR?

REPROCESSED ENDOSCOPIC TROCAR is a medical device that received FDA 510(k) clearance on 2006-05-23. The listed applicant is Sterilmed, Inc.. The 510(k) number is K052299.

When did REPROCESSED ENDOSCOPIC TROCAR receive FDA 510(k) clearance?

REPROCESSED ENDOSCOPIC TROCAR received FDA 510(k) clearance on 2006-05-23, under 510(k) number K052299.

Who is the listed applicant for REPROCESSED ENDOSCOPIC TROCAR?

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 ENDOSCOPIC TROCAR?

The FDA product code for REPROCESSED ENDOSCOPIC TROCAR is NLM.

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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.