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FDA 510(k)

BLOOD-SOLUTION ADMINISTRATION SET, SURG.

K-Number: K760483 · 1976-09-03

ApplicantTravenol Laboratories, S.A.
Decision Date1976-09-03
Product CodeKZD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BLOOD-SOLUTION ADMINISTRATION SET, SURG. 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 1976-09-03 under 510(k) number K760483. The device is classified under product code KZD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD-SOLUTION ADMINISTRATION SET, SURG.?

BLOOD-SOLUTION ADMINISTRATION SET, SURG. is a medical device that received FDA 510(k) clearance on 1976-09-03. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K760483.

When did BLOOD-SOLUTION ADMINISTRATION SET, SURG. receive FDA 510(k) clearance?

BLOOD-SOLUTION ADMINISTRATION SET, SURG. received FDA 510(k) clearance on 1976-09-03, under 510(k) number K760483.

Who is the listed applicant for BLOOD-SOLUTION ADMINISTRATION SET, SURG.?

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 BLOOD-SOLUTION ADMINISTRATION SET, SURG.?

The FDA product code for BLOOD-SOLUTION ADMINISTRATION SET, SURG. is KZD.

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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: KZD)

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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