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FDA 510(k)

TRAVASORB NASOGASTRIC NASOINTESTINAL

K-Number: K823082 · 1982-11-16

ApplicantTravenol Laboratories, S.A.
Decision Date1982-11-16
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TRAVASORB NASOGASTRIC NASOINTESTINAL 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 1982-11-16 under 510(k) number K823082. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAVASORB NASOGASTRIC NASOINTESTINAL?

TRAVASORB NASOGASTRIC NASOINTESTINAL is a medical device that received FDA 510(k) clearance on 1982-11-16. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K823082.

When did TRAVASORB NASOGASTRIC NASOINTESTINAL receive FDA 510(k) clearance?

TRAVASORB NASOGASTRIC NASOINTESTINAL received FDA 510(k) clearance on 1982-11-16, under 510(k) number K823082.

Who is the listed applicant for TRAVASORB NASOGASTRIC NASOINTESTINAL?

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 TRAVASORB NASOGASTRIC NASOINTESTINAL?

The FDA product code for TRAVASORB NASOGASTRIC NASOINTESTINAL is KNT.

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Other records listing Travenol Laboratories, S.A. as applicant

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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: KNT)

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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