CHLAMYDIA GROUP CF ANTIGEN
K-Number: K844868 · 1985-03-05
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Device Summary
Frequently Asked Questions
What is the CHLAMYDIA GROUP CF ANTIGEN?
CHLAMYDIA GROUP CF ANTIGEN is a medical device that received FDA 510(k) clearance on 1985-03-05. The listed applicant is Hillcrest Biologicals. The 510(k) number is K844868.
When did CHLAMYDIA GROUP CF ANTIGEN receive FDA 510(k) clearance?
CHLAMYDIA GROUP CF ANTIGEN received FDA 510(k) clearance on 1985-03-05, under 510(k) number K844868.
Who is the listed applicant for CHLAMYDIA GROUP CF ANTIGEN?
The FDA 510(k) record lists Hillcrest Biologicals as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHLAMYDIA GROUP CF ANTIGEN?
The FDA product code for CHLAMYDIA GROUP CF ANTIGEN is GPW.
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 Hillcrest Biologicals 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: GPW)
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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