INJECTION SITE #014456-120
K-Number: K870913 · 1987-03-17
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Device Summary
Frequently Asked Questions
What is the INJECTION SITE #014456-120?
INJECTION SITE #014456-120 is a medical device that received FDA 510(k) clearance on 1987-03-17. The listed applicant is Clinical Connections, Inc.. The 510(k) number is K870913.
When did INJECTION SITE #014456-120 receive FDA 510(k) clearance?
INJECTION SITE #014456-120 received FDA 510(k) clearance on 1987-03-17, under 510(k) number K870913.
Who is the listed applicant for INJECTION SITE #014456-120?
The FDA 510(k) record lists Clinical Connections, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INJECTION SITE #014456-120?
The FDA product code for INJECTION SITE #014456-120 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 Clinical Connections, 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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