INTRAVENOUS FILTER W/AUTO AIR VENT
K-Number: K771826 · 1977-10-13
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Device Summary
Frequently Asked Questions
What is the INTRAVENOUS FILTER W/AUTO AIR VENT?
INTRAVENOUS FILTER W/AUTO AIR VENT 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 K771826.
When did INTRAVENOUS FILTER W/AUTO AIR VENT receive FDA 510(k) clearance?
INTRAVENOUS FILTER W/AUTO AIR VENT received FDA 510(k) clearance on 1977-10-13, under 510(k) number K771826.
Who is the listed applicant for INTRAVENOUS FILTER W/AUTO AIR VENT?
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 INTRAVENOUS FILTER W/AUTO AIR VENT?
The FDA product code for INTRAVENOUS FILTER W/AUTO AIR VENT is FPB.
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: FPB)
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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