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FDA 510(k)

TRAVENOL FLO-GARD 500 IV MONITOR

K-Number: K850710 · 1985-04-04

ApplicantTravenol Laboratories, S.A.
Decision Date1985-04-04
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRAVENOL FLO-GARD 500 IV MONITOR 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 1985-04-04 under 510(k) number K850710. The device is classified under product code FLN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAVENOL FLO-GARD 500 IV MONITOR?

TRAVENOL FLO-GARD 500 IV MONITOR is a medical device that received FDA 510(k) clearance on 1985-04-04. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K850710.

When did TRAVENOL FLO-GARD 500 IV MONITOR receive FDA 510(k) clearance?

TRAVENOL FLO-GARD 500 IV MONITOR received FDA 510(k) clearance on 1985-04-04, under 510(k) number K850710.

Who is the listed applicant for TRAVENOL FLO-GARD 500 IV MONITOR?

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 TRAVENOL FLO-GARD 500 IV MONITOR?

The FDA product code for TRAVENOL FLO-GARD 500 IV MONITOR is FLN.

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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: FLN)

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.

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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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