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FDA 510(k)

1.2 MICRON AIR ELIMINATING FILTER

K-Number: K942625 · 1994-10-07

ApplicantThe Medi-Dose Group
Decision Date1994-10-07
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

1.2 MICRON AIR ELIMINATING FILTER is the device name listed in this FDA 510(k) record. The listed applicant is The Medi-Dose Group. It received FDA 510(k) clearance on 1994-10-07 under 510(k) number K942625. 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 1.2 MICRON AIR ELIMINATING FILTER?

1.2 MICRON AIR ELIMINATING FILTER is a medical device that received FDA 510(k) clearance on 1994-10-07. The listed applicant is The Medi-Dose Group. The 510(k) number is K942625.

When did 1.2 MICRON AIR ELIMINATING FILTER receive FDA 510(k) clearance?

1.2 MICRON AIR ELIMINATING FILTER received FDA 510(k) clearance on 1994-10-07, under 510(k) number K942625.

Who is the listed applicant for 1.2 MICRON AIR ELIMINATING FILTER?

The FDA 510(k) record lists The Medi-Dose Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 1.2 MICRON AIR ELIMINATING FILTER?

The FDA product code for 1.2 MICRON AIR ELIMINATING FILTER is FPB.

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Other records listing The Medi-Dose Group 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.

K952242TRANSFEER SPIKE IIK900651TS-1800 MEDICATION TRANSFER SPIKEK895291IV DISPESNSING SPIKEK895290CHEMO-SPIKE RECONSTITUTION DEVICEK896291INJECTION PORT II --- FOR INTERMITTENT INJECTIONK895419DISPOSABLE DISC FILTER

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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.

K261403Lipipor NLF1A Infusion Filter, Lipipor NLF2A & NLF2NTA Infusion Filters, Lipipor TNA2A Infusion FilterGlobal Life Sciences Solutions USA, LLCK233277Filter Needle for Single UseHangzhou Qiantang Longyue Biotechnology Co., Ltd.K113227NON-DEHP MICRO-VOLUME EXTENSION SET WITH 0.22 MICRON FILTERBaxter Healthcare CorpK021293ARTERIA BLOOD FILTERArteria Medical Science, Inc.K993379PALL SUPOR AEF FILTERPall Corp.K9746610.2 U BACTERIAL FILTERSims Deltec, Inc.

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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