PHARMACIA B2 MICRO EIA
K-Number: K900449 · 1990-02-05
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Device Summary
Frequently Asked Questions
What is the PHARMACIA B2 MICRO EIA?
PHARMACIA B2 MICRO EIA is a medical device that received FDA 510(k) clearance on 1990-02-05. The listed applicant is Pharmacia, Inc.. The 510(k) number is K900449.
When did PHARMACIA B2 MICRO EIA receive FDA 510(k) clearance?
PHARMACIA B2 MICRO EIA received FDA 510(k) clearance on 1990-02-05, under 510(k) number K900449.
Who is the listed applicant for PHARMACIA B2 MICRO EIA?
The FDA 510(k) record lists Pharmacia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHARMACIA B2 MICRO EIA?
The FDA product code for PHARMACIA B2 MICRO EIA is JZG.
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 Pharmacia, Inc. 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: JZG)
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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