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FDA 510(k)

REPROCESSED TROCARS AND CANNULAS

K-Number: K012644 · 2002-07-29

Decision Date2002-07-29
Product CodeNLM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED TROCARS AND CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Instruments Service and Savings, Inc.. It received FDA 510(k) clearance on 2002-07-29 under 510(k) number K012644. 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 TROCARS AND CANNULAS?

REPROCESSED TROCARS AND CANNULAS is a medical device that received FDA 510(k) clearance on 2002-07-29. The listed applicant is Surgical Instruments Service and Savings, Inc.. The 510(k) number is K012644.

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

REPROCESSED TROCARS AND CANNULAS received FDA 510(k) clearance on 2002-07-29, under 510(k) number K012644.

Who is the listed applicant for REPROCESSED TROCARS AND CANNULAS?

The FDA 510(k) record lists Surgical Instruments Service and Savings, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Clinical Trials

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.

Other records listing Surgical Instruments Service and Savings, Inc. 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.

View all 7 devices →

Related Devices (Code: NLM)

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.

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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