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FDA 510(k)

REPROCESSED IMAGING CATHETERS

K-Number: K012537 · 2002-10-11

Decision Date2002-10-11
Product CodeOWQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REPROCESSED IMAGING CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2002-10-11 under 510(k) number K012537. The device is classified under product code OWQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED IMAGING CATHETERS?

REPROCESSED IMAGING CATHETERS is a medical device that received FDA 510(k) clearance on 2002-10-11. The listed applicant is Sterilmed, Inc.. The 510(k) number is K012537.

When did REPROCESSED IMAGING CATHETERS receive FDA 510(k) clearance?

REPROCESSED IMAGING CATHETERS received FDA 510(k) clearance on 2002-10-11, under 510(k) number K012537.

Who is the listed applicant for REPROCESSED IMAGING CATHETERS?

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 IMAGING CATHETERS?

The FDA product code for REPROCESSED IMAGING CATHETERS is OWQ.

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 Sterilmed, 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.

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Related Devices (Code: OWQ)

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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