BURETTE INTRAVENOUS ADMIN. SETS.
K-Number: K780130 · 1978-02-21
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Device Summary
Frequently Asked Questions
What is the BURETTE INTRAVENOUS ADMIN. SETS.?
BURETTE INTRAVENOUS ADMIN. SETS. is a medical device that received FDA 510(k) clearance on 1978-02-21. The listed applicant is Y. The 510(k) number is K780130.
When did BURETTE INTRAVENOUS ADMIN. SETS. receive FDA 510(k) clearance?
BURETTE INTRAVENOUS ADMIN. SETS. received FDA 510(k) clearance on 1978-02-21, under 510(k) number K780130.
Who is the listed applicant for BURETTE INTRAVENOUS ADMIN. SETS.?
The FDA 510(k) record lists Y as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BURETTE INTRAVENOUS ADMIN. SETS.?
The FDA product code for BURETTE INTRAVENOUS ADMIN. SETS. is FPA.
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 Y 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: FPA)
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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