MICROFILTRATION SET MF10
K-Number: K770253 · 1977-04-05
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Device Summary
Frequently Asked Questions
What is the MICROFILTRATION SET MF10?
MICROFILTRATION SET MF10 is a medical device that received FDA 510(k) clearance on 1977-04-05. The listed applicant is Biotest-Serum-Institut. The 510(k) number is K770253.
When did MICROFILTRATION SET MF10 receive FDA 510(k) clearance?
MICROFILTRATION SET MF10 received FDA 510(k) clearance on 1977-04-05, under 510(k) number K770253.
Who is the listed applicant for MICROFILTRATION SET MF10?
The FDA 510(k) record lists Biotest-Serum-Institut as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROFILTRATION SET MF10?
The FDA product code for MICROFILTRATION SET MF10 is CAK.
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 Biotest-Serum-Institut 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: CAK)
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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