BUN-UN CENTRIFICHUM 500, #65080/81
K-Number: K823300 · 1983-01-09
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Device Summary
Frequently Asked Questions
What is the BUN-UN CENTRIFICHUM 500, #65080/81?
BUN-UN CENTRIFICHUM 500, #65080/81 is a medical device that received FDA 510(k) clearance on 1983-01-09. The listed applicant is Emd Chemicals, Inc.. The 510(k) number is K823300.
When did BUN-UN CENTRIFICHUM 500, #65080/81 receive FDA 510(k) clearance?
BUN-UN CENTRIFICHUM 500, #65080/81 received FDA 510(k) clearance on 1983-01-09, under 510(k) number K823300.
Who is the listed applicant for BUN-UN CENTRIFICHUM 500, #65080/81?
The FDA 510(k) record lists Emd Chemicals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BUN-UN CENTRIFICHUM 500, #65080/81?
The FDA product code for BUN-UN CENTRIFICHUM 500, #65080/81 is CDQ.
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 Emd Chemicals, Inc. 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: CDQ)
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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