ESTRADIOL MAIACLONE RADIOIMMUNOASSAY KIT
K-Number: K890645 · 1989-03-08
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Device Summary
Frequently Asked Questions
What is the ESTRADIOL MAIACLONE RADIOIMMUNOASSAY KIT?
ESTRADIOL MAIACLONE RADIOIMMUNOASSAY KIT is a medical device that received FDA 510(k) clearance on 1989-03-08. The listed applicant is Serono-Baker Diagnostics, Inc.. The 510(k) number is K890645.
When did ESTRADIOL MAIACLONE RADIOIMMUNOASSAY KIT receive FDA 510(k) clearance?
ESTRADIOL MAIACLONE RADIOIMMUNOASSAY KIT received FDA 510(k) clearance on 1989-03-08, under 510(k) number K890645.
Who is the listed applicant for ESTRADIOL MAIACLONE RADIOIMMUNOASSAY KIT?
The FDA 510(k) record lists Serono-Baker Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ESTRADIOL MAIACLONE RADIOIMMUNOASSAY KIT?
The FDA product code for ESTRADIOL MAIACLONE RADIOIMMUNOASSAY KIT is CHP.
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 Serono-Baker Diagnostics, 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: CHP)
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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