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FDA 510(k)

NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS

K-Number: K021080 · 2002-08-29

Decision Date2002-08-29
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Cardio Med Supplies, Inc.. It received FDA 510(k) clearance on 2002-08-29 under 510(k) number K021080. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS?

NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS is a medical device that received FDA 510(k) clearance on 2002-08-29. The listed applicant is Cardio Med Supplies, Inc.. The 510(k) number is K021080.

When did NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS receive FDA 510(k) clearance?

NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS received FDA 510(k) clearance on 2002-08-29, under 510(k) number K021080.

Who is the listed applicant for NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS?

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

What is the FDA product code for NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS?

The FDA product code for NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS is FPA.

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 Cardio Med 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.

Related Devices (Code: FPA)

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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