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FDA 510(k)

STERILEMED REPROCESSED IVUS IMAGING CATHETER

K-Number: K043453 · 2005-03-01

ApplicantSterilmed, Inc.
Decision Date2005-03-01
Product CodeOWQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STERILEMED REPROCESSED IVUS IMAGING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2005-03-01 under 510(k) number K043453. 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 STERILEMED REPROCESSED IVUS IMAGING CATHETER?

STERILEMED REPROCESSED IVUS IMAGING CATHETER is a medical device that received FDA 510(k) clearance on 2005-03-01. The listed applicant is Sterilmed, Inc.. The 510(k) number is K043453.

When did STERILEMED REPROCESSED IVUS IMAGING CATHETER receive FDA 510(k) clearance?

STERILEMED REPROCESSED IVUS IMAGING CATHETER received FDA 510(k) clearance on 2005-03-01, under 510(k) number K043453.

Who is the listed applicant for STERILEMED REPROCESSED IVUS IMAGING CATHETER?

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 STERILEMED REPROCESSED IVUS IMAGING CATHETER?

The FDA product code for STERILEMED REPROCESSED IVUS IMAGING CATHETER is OWQ.

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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.

K254149Reprocessed AcuNav CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on Siemens System (R11510825); Reprocessed AcuNav CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on GE System (R11657484); Reprocessed SOUNDSTAR CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on Siemens System (R11510826); Reprocessed SOUNDSTAR CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on GE System (R11657485)Sterilmed, Inc.K250545Medline ReNewal Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter (8F, 8FG, 10F, 10FG)Surgical Instrument Service and Savings, Inc.K250592NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)Northeast Scientific, Inc.K243101Medline ReNewal Reprocessed Siemens ACUSON AcuNav 10F Ultrasound Catheter (for Siemens Systems) (08255790 ); Medline ReNewal Reprocessed Siemens ACUSON AcuNav 10F Ultrasound Catheter (for GE Systems) (10043342)Surgical Instrument Service and Savings, Inc.K234064Medline ReNewal Reprocessed Siemens ACUSON AcuNav 8F Ultrasound Catheter (for Siemens Systems) (10135936); Medline ReNewal Reprocessed Siemens ACUSON AcuNav 8F Ultrasound Catheter (for GE Systems) (10135910)Surgical Instrument Service and Savings, Inc.K232130Medline ReNewal Reprocessed ViewFlex Xtra ICE CatheterSurgical Instrument Services and Savings, 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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