DISPOSABLE DISC FILTER
K-Number: K936015 · 1994-12-12
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE DISC FILTER?
DISPOSABLE DISC FILTER is a medical device that received FDA 510(k) clearance on 1994-12-12. The listed applicant is Medi-Dose, Inc.. The 510(k) number is K936015.
When did DISPOSABLE DISC FILTER receive FDA 510(k) clearance?
DISPOSABLE DISC FILTER received FDA 510(k) clearance on 1994-12-12, under 510(k) number K936015.
Who is the listed applicant for DISPOSABLE DISC FILTER?
The FDA 510(k) record lists Medi-Dose, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE DISC FILTER?
The FDA product code for DISPOSABLE DISC FILTER is FMF.
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 Medi-Dose, 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: FMF)
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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