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FDA 510(k)

MODIFICATION TO:INTRODUCER SETS, MODEL ADELANTE AND ADELANTE-S

K-Number: K090114 · 2009-06-04

ApplicantOscor, Inc.
Decision Date2009-06-04
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO:INTRODUCER SETS, MODEL ADELANTE AND ADELANTE-S is the device name listed in this FDA 510(k) record. The listed applicant is Oscor, Inc.. It received FDA 510(k) clearance on 2009-06-04 under 510(k) number K090114. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO:INTRODUCER SETS, MODEL ADELANTE AND ADELANTE-S?

MODIFICATION TO:INTRODUCER SETS, MODEL ADELANTE AND ADELANTE-S is a medical device that received FDA 510(k) clearance on 2009-06-04. The listed applicant is Oscor, Inc.. The 510(k) number is K090114.

When did MODIFICATION TO:INTRODUCER SETS, MODEL ADELANTE AND ADELANTE-S receive FDA 510(k) clearance?

MODIFICATION TO:INTRODUCER SETS, MODEL ADELANTE AND ADELANTE-S received FDA 510(k) clearance on 2009-06-04, under 510(k) number K090114.

Who is the listed applicant for MODIFICATION TO:INTRODUCER SETS, MODEL ADELANTE AND ADELANTE-S?

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

What is the FDA product code for MODIFICATION TO:INTRODUCER SETS, MODEL ADELANTE AND ADELANTE-S?

The FDA product code for MODIFICATION TO:INTRODUCER SETS, MODEL ADELANTE AND ADELANTE-S is DYB.

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 Oscor, 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: DYB)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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