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)

CONDUIT TCP GRANULES

K-Number: K014053 · 2002-03-08

ApplicantDepuyacromed
Decision Date2002-03-08
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONDUIT TCP GRANULES is the device name listed in this FDA 510(k) record. The listed applicant is Depuyacromed. It received FDA 510(k) clearance on 2002-03-08 under 510(k) number K014053. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONDUIT TCP GRANULES?

CONDUIT TCP GRANULES is a medical device that received FDA 510(k) clearance on 2002-03-08. The listed applicant is Depuyacromed. The 510(k) number is K014053.

When did CONDUIT TCP GRANULES receive FDA 510(k) clearance?

CONDUIT TCP GRANULES received FDA 510(k) clearance on 2002-03-08, under 510(k) number K014053.

Who is the listed applicant for CONDUIT TCP GRANULES?

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

What is the FDA product code for CONDUIT TCP GRANULES?

The FDA product code for CONDUIT TCP GRANULES is MQV.

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 Depuyacromed 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 48 devices →

Related Devices (Code: MQV)

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.

↑