PORT ACCESS KITS
K-Number: K872011 · 1987-07-13
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Device Summary
Frequently Asked Questions
What is the PORT ACCESS KITS?
PORT ACCESS KITS is a medical device that received FDA 510(k) clearance on 1987-07-13. The listed applicant is The Jarid Group, Inc.. The 510(k) number is K872011.
When did PORT ACCESS KITS receive FDA 510(k) clearance?
PORT ACCESS KITS received FDA 510(k) clearance on 1987-07-13, under 510(k) number K872011.
Who is the listed applicant for PORT ACCESS KITS?
The FDA 510(k) record lists The Jarid Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PORT ACCESS KITS?
The FDA product code for PORT ACCESS KITS is LRO.
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 The Jarid Group, 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: LRO)
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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