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FDA 510(k)

CUTTER PUREFLO PLUS IV FILTER

K-Number: K872634 · 1987-08-04

ApplicantMiles Laboratories, Inc.
Decision Date1987-08-04
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CUTTER PUREFLO PLUS IV FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Miles Laboratories, Inc.. It received FDA 510(k) clearance on 1987-08-04 under 510(k) number K872634. 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 CUTTER PUREFLO PLUS IV FILTER?

CUTTER PUREFLO PLUS IV FILTER is a medical device that received FDA 510(k) clearance on 1987-08-04. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K872634.

When did CUTTER PUREFLO PLUS IV FILTER receive FDA 510(k) clearance?

CUTTER PUREFLO PLUS IV FILTER received FDA 510(k) clearance on 1987-08-04, under 510(k) number K872634.

Who is the listed applicant for CUTTER PUREFLO PLUS IV FILTER?

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

What is the FDA product code for CUTTER PUREFLO PLUS IV FILTER?

The FDA product code for CUTTER PUREFLO PLUS IV FILTER is FPB.

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Other records listing Miles Laboratories, 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.

K880605LABELING CHANGE FOR CUTTER PUREFLO PLUS IV FILTERK874909MICRO-BUMINTEST REAGENT TABLETSK875079MODIFIED SERALYZER ALT/SGPT REAG. STRIPS & MODULEK871835GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINTK872120SERALYZER III BLOOD CHEMISTRY ANALYZERK873304CLINITEK AUTO 2000 REAGENT CASSETTE (LEUKOCYTES)

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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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