CITRATE BUFFER
K-Number: K811251 · 1981-05-21
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Device Summary
Frequently Asked Questions
What is the CITRATE BUFFER?
CITRATE BUFFER is a medical device that received FDA 510(k) clearance on 1981-05-21. The listed applicant is Bioscientific. The 510(k) number is K811251.
When did CITRATE BUFFER receive FDA 510(k) clearance?
CITRATE BUFFER received FDA 510(k) clearance on 1981-05-21, under 510(k) number K811251.
Who is the listed applicant for CITRATE BUFFER?
The FDA 510(k) record lists Bioscientific as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CITRATE BUFFER?
The FDA product code for CITRATE BUFFER is JCC.
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 Bioscientific 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: JCC)
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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