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FDA 510(k)

DISC 120 TRANSPORTER

K-Number: K801391 · 1980-07-14

ApplicantTravenol Laboratories, S.A.
Decision Date1980-07-14
Product CodeJZW
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

DISC 120 TRANSPORTER 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 1980-07-14 under 510(k) number K801391. The device is classified under product code JZW. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISC 120 TRANSPORTER?

DISC 120 TRANSPORTER is a medical device that received FDA 510(k) clearance on 1980-07-14. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K801391.

When did DISC 120 TRANSPORTER receive FDA 510(k) clearance?

DISC 120 TRANSPORTER received FDA 510(k) clearance on 1980-07-14, under 510(k) number K801391.

Who is the listed applicant for DISC 120 TRANSPORTER?

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 DISC 120 TRANSPORTER?

The FDA product code for DISC 120 TRANSPORTER is JZW.

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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: JZW)

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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