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FDA 510(k)

CENTRAL VEIN CATHERIZATION KIT W/WITHOUT MEDICA.

K-Number: K870411 · 1987-06-02

Decision Date1987-06-02
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRAL VEIN CATHERIZATION KIT W/WITHOUT MEDICA. is the device name listed in this FDA 510(k) record. The listed applicant is Medical Surgical Concepts, Inc.. It received FDA 510(k) clearance on 1987-06-02 under 510(k) number K870411. 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 CENTRAL VEIN CATHERIZATION KIT W/WITHOUT MEDICA.?

CENTRAL VEIN CATHERIZATION KIT W/WITHOUT MEDICA. is a medical device that received FDA 510(k) clearance on 1987-06-02. The listed applicant is Medical Surgical Concepts, Inc.. The 510(k) number is K870411.

When did CENTRAL VEIN CATHERIZATION KIT W/WITHOUT MEDICA. receive FDA 510(k) clearance?

CENTRAL VEIN CATHERIZATION KIT W/WITHOUT MEDICA. received FDA 510(k) clearance on 1987-06-02, under 510(k) number K870411.

Who is the listed applicant for CENTRAL VEIN CATHERIZATION KIT W/WITHOUT MEDICA.?

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

What is the FDA product code for CENTRAL VEIN CATHERIZATION KIT W/WITHOUT MEDICA.?

The FDA product code for CENTRAL VEIN CATHERIZATION KIT W/WITHOUT MEDICA. is DQY.

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 Medical Surgical Concepts, 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.

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

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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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