NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS
K-Number: K021080 · 2002-08-29
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Device Summary
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
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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