FILTER TUBE
K-Number: K780519 · 1978-05-09
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Device Summary
Frequently Asked Questions
What is the FILTER TUBE?
FILTER TUBE is a medical device that received FDA 510(k) clearance on 1978-05-09. The listed applicant is Jelco Laboratories. The 510(k) number is K780519.
When did FILTER TUBE receive FDA 510(k) clearance?
FILTER TUBE received FDA 510(k) clearance on 1978-05-09, under 510(k) number K780519.
Who is the listed applicant for FILTER TUBE?
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 FILTER TUBE?
The FDA product code for FILTER TUBE is BSN.
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: BSN)
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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