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FDA 510(k)

CONTINU-FLO Y-TYPE SOLUTION ADMIN. SET

K-Number: K771498 · 1977-08-19

ApplicantTravenol Laboratories, S.A.
Decision Date1977-08-19
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONTINU-FLO Y-TYPE SOLUTION ADMIN. SET 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 1977-08-19 under 510(k) number K771498. 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 Y-TYPE SOLUTION ADMIN. SET?

CONTINU-FLO Y-TYPE SOLUTION ADMIN. SET is a medical device that received FDA 510(k) clearance on 1977-08-19. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K771498.

When did CONTINU-FLO Y-TYPE SOLUTION ADMIN. SET receive FDA 510(k) clearance?

CONTINU-FLO Y-TYPE SOLUTION ADMIN. SET received FDA 510(k) clearance on 1977-08-19, under 510(k) number K771498.

Who is the listed applicant for CONTINU-FLO Y-TYPE SOLUTION ADMIN. SET?

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 Y-TYPE SOLUTION ADMIN. SET?

The FDA product code for CONTINU-FLO Y-TYPE SOLUTION ADMIN. SET 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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