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FDA 510(k)

DISPOSABLE SCALP VEIN INFUSION SET

K-Number: K953252 · 1996-11-26

Decision Date1996-11-26
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SCALP VEIN INFUSION SET 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 1996-11-26 under 510(k) number K953252. 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 DISPOSABLE SCALP VEIN INFUSION SET?

DISPOSABLE SCALP VEIN INFUSION SET is a medical device that received FDA 510(k) clearance on 1996-11-26. The listed applicant is Myco Medical Supplies, Inc.. The 510(k) number is K953252.

When did DISPOSABLE SCALP VEIN INFUSION SET receive FDA 510(k) clearance?

DISPOSABLE SCALP VEIN INFUSION SET received FDA 510(k) clearance on 1996-11-26, under 510(k) number K953252.

Who is the listed applicant for DISPOSABLE SCALP VEIN INFUSION SET?

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 DISPOSABLE SCALP VEIN INFUSION SET?

The FDA product code for DISPOSABLE SCALP VEIN INFUSION SET 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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