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FDA 510(k)

2 MICRON AIR ELIMINATING FILTER

K-Number: K942532 · 1994-08-17

Decision Date1994-08-17
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

2 MICRON AIR ELIMINATING FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Dose, Inc.. It received FDA 510(k) clearance on 1994-08-17 under 510(k) number K942532. The device is classified under product code FPB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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