IV CATHETER HUB
K-Number: K771381 · 1977-10-13
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Device Summary
Frequently Asked Questions
What is the IV CATHETER HUB?
IV CATHETER HUB is a medical device that received FDA 510(k) clearance on 1977-10-13. The listed applicant is Jelco Laboratories. The 510(k) number is K771381.
When did IV CATHETER HUB receive FDA 510(k) clearance?
IV CATHETER HUB received FDA 510(k) clearance on 1977-10-13, under 510(k) number K771381.
Who is the listed applicant for IV CATHETER HUB?
The FDA 510(k) record lists Jelco Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IV CATHETER HUB?
The FDA product code for IV CATHETER HUB is FOZ.
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 Jelco Laboratories 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: FOZ)
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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