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FDA 510(k)

E-VAC BLOOD CULTURE SYSTEM

K-Number: K802408 · 1980-10-23

Decision Date1980-10-23
Product CodeJSC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

E-VAC BLOOD CULTURE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer Pharmaceuticals. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802408. The device is classified under product code JSC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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