ACU-MED RED MISER HEMOTHORAX BLOOD COLL.
K-Number: K791891 · 1979-12-05
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Device Summary
Frequently Asked Questions
What is the ACU-MED RED MISER HEMOTHORAX BLOOD COLL.?
ACU-MED RED MISER HEMOTHORAX BLOOD COLL. is a medical device that received FDA 510(k) clearance on 1979-12-05. The listed applicant is Acumed Instruments Corp.. The 510(k) number is K791891.
When did ACU-MED RED MISER HEMOTHORAX BLOOD COLL. receive FDA 510(k) clearance?
ACU-MED RED MISER HEMOTHORAX BLOOD COLL. received FDA 510(k) clearance on 1979-12-05, under 510(k) number K791891.
Who is the listed applicant for ACU-MED RED MISER HEMOTHORAX BLOOD COLL.?
The FDA 510(k) record lists Acumed Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACU-MED RED MISER HEMOTHORAX BLOOD COLL.?
The FDA product code for ACU-MED RED MISER HEMOTHORAX BLOOD COLL. is CAC.
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 Acumed Instruments Corp. 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: CAC)
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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