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FDA 510(k)

MODEL 40-30-2 AIR ELIMINATING FILTER SET

K-Number: K801614 · 1980-08-13

ApplicantY
Decision Date1980-08-13
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 40-30-2 AIR ELIMINATING FILTER SET is the device name listed in this FDA 510(k) record. The listed applicant is Y. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801614. 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 MODEL 40-30-2 AIR ELIMINATING FILTER SET?

MODEL 40-30-2 AIR ELIMINATING FILTER SET is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is Y. The 510(k) number is K801614.

When did MODEL 40-30-2 AIR ELIMINATING FILTER SET receive FDA 510(k) clearance?

MODEL 40-30-2 AIR ELIMINATING FILTER SET received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801614.

Who is the listed applicant for MODEL 40-30-2 AIR ELIMINATING FILTER SET?

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

What is the FDA product code for MODEL 40-30-2 AIR ELIMINATING FILTER SET?

The FDA product code for MODEL 40-30-2 AIR ELIMINATING FILTER SET is FPB.

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Other records listing Y 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.

K955846MODEL 2082 TEMP PLUS III THERMOMETER/MODEL 2087 TEMP PLUS III WALL MOUNT THERMOMETERK960280IVAC NEEDLE FREE VALVE ADMINISTRATION SETSK953225IVAC BALL VALCE ADMIN. SETSK934095IVAC VENTED SYRINGE ADAPTER ADMINISTRATION SETSK940897IVAC NEEDLELESS INFECTION VALVE ADMINISTRATION SETK931550EZ ADMINISTRATION SET

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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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