FDA 510(k)

DESERET I.V. FILTER

K-Number: K801602 · 1980-08-27

Decision Date1980-08-27

Product CodeFPB

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

DESERET I.V. FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Hospital Products Co.. It received FDA 510(k) clearance on 1980-08-27 under 510(k) number K801602. 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 DESERET I.V. FILTER?

DESERET I.V. FILTER is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Hospital Products Co.. The 510(k) number is K801602.

When did DESERET I.V. FILTER receive FDA 510(k) clearance?

DESERET I.V. FILTER received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801602.

Who is the listed applicant for DESERET I.V. FILTER?

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

What is the FDA product code for DESERET I.V. FILTER?

The FDA product code for DESERET I.V. FILTER is FPB.

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Other records listing Hospital Products Co. as applicant

K823696MICRO Z BLOOD COLLECTING NEEDLES K810318PARKE-DAVIS NON-WOVEN SPONGE K801173ANGIO-FLO MONITORING KIT K792386NUTRA-PH INSTRUMENT MILK K791350POPE AMBULATORY HALO VEST

Related Devices (Code: FPB)

K261403Lipipor NLF1A Infusion Filter, Lipipor NLF2A & NLF2NTA Infusion Filters, Lipipor TNA2A Infusion FilterGlobal Life Sciences Solutions USA, LLC K233277Filter Needle for Single UseHangzhou Qiantang Longyue Biotechnology Co., Ltd.K113227NON-DEHP MICRO-VOLUME EXTENSION SET WITH 0.22 MICRON FILTERBaxter Healthcare Corp K021293ARTERIA BLOOD FILTERArteria Medical Science, Inc.K993379PALL SUPOR AEF FILTERPall Corp.K9746610.2 U BACTERIAL FILTERSims Deltec, Inc.

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.