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FDA 510(k)

CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER

K-Number: K865029 · 1987-04-17

ApplicantTravenol Laboratories, S.A.
Decision Date1987-04-17
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1987-04-17 under 510(k) number K865029. 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 CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER?

CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER is a medical device that received FDA 510(k) clearance on 1987-04-17. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K865029.

When did CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER receive FDA 510(k) clearance?

CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER received FDA 510(k) clearance on 1987-04-17, under 510(k) number K865029.

Who is the listed applicant for CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER?

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

What is the FDA product code for CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER?

The FDA product code for CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER is FPB.

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Other records listing Travenol Laboratories, S.A. 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.

K874181BAXTER BEDSIDE SYSTEMK873894CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITEK873873RESUBMITTED MICRON TRANSFUSION FILTERK873984AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)K872364HEMODIALYSIS (SPS), MODEL 550, CODE 5M1309K872652UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEM

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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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