HEMOX-ANALYZER
K-Number: K771253 · 1977-08-25
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Device Summary
Frequently Asked Questions
What is the HEMOX-ANALYZER?
HEMOX-ANALYZER is a medical device that received FDA 510(k) clearance on 1977-08-25. The listed applicant is 3M Company. The 510(k) number is K771253.
When did HEMOX-ANALYZER receive FDA 510(k) clearance?
HEMOX-ANALYZER received FDA 510(k) clearance on 1977-08-25, under 510(k) number K771253.
Who is the listed applicant for HEMOX-ANALYZER?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMOX-ANALYZER?
The FDA product code for HEMOX-ANALYZER is CHL.
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 3M Company 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: CHL)
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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