E-VAC BLOOD CULTURE SYSTEM
K-Number: K802408 · 1980-10-23
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Device Summary
Frequently Asked Questions
What is the E-VAC BLOOD CULTURE SYSTEM?
E-VAC BLOOD CULTURE SYSTEM is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Pfizer Pharmaceuticals. The 510(k) number is K802408.
When did E-VAC BLOOD CULTURE SYSTEM receive FDA 510(k) clearance?
E-VAC BLOOD CULTURE SYSTEM received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802408.
Who is the listed applicant for E-VAC BLOOD CULTURE SYSTEM?
The FDA 510(k) record lists Pfizer Pharmaceuticals as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for E-VAC BLOOD CULTURE SYSTEM?
The FDA product code for E-VAC BLOOD CULTURE SYSTEM is JSC.
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 Pfizer Pharmaceuticals 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: JSC)
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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