PHARMACIA B2-MICRO RIA
K-Number: K880719 · 1988-04-21
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Device Summary
Frequently Asked Questions
What is the PHARMACIA B2-MICRO RIA?
PHARMACIA B2-MICRO RIA is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Pharmacia, Inc.. The 510(k) number is K880719.
When did PHARMACIA B2-MICRO RIA receive FDA 510(k) clearance?
PHARMACIA B2-MICRO RIA received FDA 510(k) clearance on 1988-04-21, under 510(k) number K880719.
Who is the listed applicant for PHARMACIA B2-MICRO RIA?
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 RIA?
The FDA product code for PHARMACIA B2-MICRO RIA 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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