INFUSION SET W/ INJECTION SITE, 23D-W
K-Number: K781187 · 1978-08-10
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Device Summary
Frequently Asked Questions
What is the INFUSION SET W/ INJECTION SITE, 23D-W?
INFUSION SET W/ INJECTION SITE, 23D-W is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is Venospital, Inc.. The 510(k) number is K781187.
When did INFUSION SET W/ INJECTION SITE, 23D-W receive FDA 510(k) clearance?
INFUSION SET W/ INJECTION SITE, 23D-W received FDA 510(k) clearance on 1978-08-10, under 510(k) number K781187.
Who is the listed applicant for INFUSION SET W/ INJECTION SITE, 23D-W?
The FDA 510(k) record lists Venospital, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INFUSION SET W/ INJECTION SITE, 23D-W?
The FDA product code for INFUSION SET W/ INJECTION SITE, 23D-W 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 Venospital, 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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