2 MICRON AIR ELIMINATING FILTER
K-Number: K942532 · 1994-08-17
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Device Summary
Frequently Asked Questions
What is the 2 MICRON AIR ELIMINATING FILTER?
2 MICRON AIR ELIMINATING FILTER is a medical device that received FDA 510(k) clearance on 1994-08-17. The listed applicant is Medi-Dose, Inc.. The 510(k) number is K942532.
When did 2 MICRON AIR ELIMINATING FILTER receive FDA 510(k) clearance?
2 MICRON AIR ELIMINATING FILTER received FDA 510(k) clearance on 1994-08-17, under 510(k) number K942532.
Who is the listed applicant for 2 MICRON AIR ELIMINATING 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 2 MICRON AIR ELIMINATING FILTER?
The FDA product code for 2 MICRON AIR ELIMINATING FILTER 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 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: 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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