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FDA 510(k)

FILTRARE TM ALLVENT TM

K-Number: K834376 · 1984-05-11

ApplicantAlltek, Inc.
Decision Date1984-05-11
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FILTRARE TM ALLVENT TM is the device name listed in this FDA 510(k) record. The listed applicant is Alltek, Inc.. It received FDA 510(k) clearance on 1984-05-11 under 510(k) number K834376. 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 FILTRARE TM ALLVENT TM?

FILTRARE TM ALLVENT TM is a medical device that received FDA 510(k) clearance on 1984-05-11. The listed applicant is Alltek, Inc.. The 510(k) number is K834376.

When did FILTRARE TM ALLVENT TM receive FDA 510(k) clearance?

FILTRARE TM ALLVENT TM received FDA 510(k) clearance on 1984-05-11, under 510(k) number K834376.

Who is the listed applicant for FILTRARE TM ALLVENT TM?

The FDA 510(k) record lists Alltek, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FILTRARE TM ALLVENT TM?

The FDA product code for FILTRARE TM ALLVENT TM 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.

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Other records listing Alltek, 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.

K854172I.V. WATCHK852030PEDIATRIC IV WATCHK852029I.V. WATCHK840495MANUAL IRRIGATING/ASPIRATING UNIT

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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