SLEEVED FILTER
K-Number: K010040 · 2001-03-09
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Device Summary
Frequently Asked Questions
What is the SLEEVED FILTER?
SLEEVED FILTER is a medical device that received FDA 510(k) clearance on 2001-03-09. The listed applicant is King Systems Corp.. The 510(k) number is K010040.
When did SLEEVED FILTER receive FDA 510(k) clearance?
SLEEVED FILTER received FDA 510(k) clearance on 2001-03-09, under 510(k) number K010040.
Who is the listed applicant for SLEEVED FILTER?
The FDA 510(k) record lists King Systems Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SLEEVED FILTER?
The FDA product code for SLEEVED FILTER is CAH.
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 King Systems Corp. 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: CAH)
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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