Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back Up

K-Number: K171653 · 2017-07-03

Decision Date2017-07-03
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back Up is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 2017-07-03 under 510(k) number K171653. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back Up?

YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back Up is a medical device that received FDA 510(k) clearance on 2017-07-03. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K171653.

When did YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back Up receive FDA 510(k) clearance?

YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back Up received FDA 510(k) clearance on 2017-07-03, under 510(k) number K171653.

Who is the listed applicant for YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back Up?

The FDA 510(k) record lists Codman & Shurtleff, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back Up?

The FDA product code for YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back Up is DQY.

Other records listing Codman & Shurtleff, 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 11 devices →

Related Devices (Code: DQY)

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.