SOLUTION ADMINISTRATION SET (#2C0631)
K-Number: K760505 · 1976-09-03
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Device Summary
Frequently Asked Questions
What is the SOLUTION ADMINISTRATION SET (#2C0631)?
SOLUTION ADMINISTRATION SET (#2C0631) 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 K760505.
When did SOLUTION ADMINISTRATION SET (#2C0631) receive FDA 510(k) clearance?
SOLUTION ADMINISTRATION SET (#2C0631) received FDA 510(k) clearance on 1976-09-03, under 510(k) number K760505.
Who is the listed applicant for SOLUTION ADMINISTRATION SET (#2C0631)?
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 SOLUTION ADMINISTRATION SET (#2C0631)?
The FDA product code for SOLUTION ADMINISTRATION SET (#2C0631) is KZD.
Related Clinical Trials
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.
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.
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.
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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