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FDA 510(k)

CATHY STERILE DISPOSABLE I.V. CANNULA WITH CATHETER

K-Number: K042504 · 2006-01-19

Decision Date2006-01-19
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATHY STERILE DISPOSABLE I.V. CANNULA WITH CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Myco Medical Supplies, Inc.. It received FDA 510(k) clearance on 2006-01-19 under 510(k) number K042504. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHY STERILE DISPOSABLE I.V. CANNULA WITH CATHETER?

CATHY STERILE DISPOSABLE I.V. CANNULA WITH CATHETER is a medical device that received FDA 510(k) clearance on 2006-01-19. The listed applicant is Myco Medical Supplies, Inc.. The 510(k) number is K042504.

When did CATHY STERILE DISPOSABLE I.V. CANNULA WITH CATHETER receive FDA 510(k) clearance?

CATHY STERILE DISPOSABLE I.V. CANNULA WITH CATHETER received FDA 510(k) clearance on 2006-01-19, under 510(k) number K042504.

Who is the listed applicant for CATHY STERILE DISPOSABLE I.V. CANNULA WITH CATHETER?

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

What is the FDA product code for CATHY STERILE DISPOSABLE I.V. CANNULA WITH CATHETER?

The FDA product code for CATHY STERILE DISPOSABLE I.V. CANNULA WITH CATHETER is FOZ.

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 Myco Medical Supplies, 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 12 devices →

Related Devices (Code: FOZ)

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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