OPUS(R) TOTAL B-HCG TEST SYSTEM
K-Number: K932279 · 1993-07-08
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Device Summary
Frequently Asked Questions
What is the OPUS(R) TOTAL B-HCG TEST SYSTEM?
OPUS(R) TOTAL B-HCG TEST SYSTEM is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Pb Diagnostic Systems, Inc.. The 510(k) number is K932279.
When did OPUS(R) TOTAL B-HCG TEST SYSTEM receive FDA 510(k) clearance?
OPUS(R) TOTAL B-HCG TEST SYSTEM received FDA 510(k) clearance on 1993-07-08, under 510(k) number K932279.
Who is the listed applicant for OPUS(R) TOTAL B-HCG TEST SYSTEM?
The FDA 510(k) record lists Pb Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPUS(R) TOTAL B-HCG TEST SYSTEM?
The FDA product code for OPUS(R) TOTAL B-HCG TEST SYSTEM is JHI.
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 Pb Diagnostic Systems, 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: JHI)
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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