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FDA 510(k)

REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS

K-Number: K024015 · 2003-03-04

ApplicantAlliance Medical Corp.
Decision Date2003-03-04
Product CodeNLM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Medical Corp.. It received FDA 510(k) clearance on 2003-03-04 under 510(k) number K024015. 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 TROCARS AND CANNULAS?

REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS is a medical device that received FDA 510(k) clearance on 2003-03-04. The listed applicant is Alliance Medical Corp.. The 510(k) number is K024015.

When did REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS receive FDA 510(k) clearance?

REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS received FDA 510(k) clearance on 2003-03-04, under 510(k) number K024015.

Who is the listed applicant for REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS?

The FDA 510(k) record lists Alliance Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS?

The FDA product code for REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS is NLM.

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Other records listing Alliance Medical Corp. as applicant

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.

K060648REPROCESSED PHACOEMULSIFICATION TIPSK061045REPROCESSED ELECTROPHYSIOLOGY CATHETERSK060049REPROCESSED COMPRESSION SLEEVESK060091ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVESK053316REPROCESSED COMPRESSION SLEEVESK052918REPROCESSED EXTERNAL FIXATION DEVICES

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Related Devices (Code: 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.

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