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FDA 510(k)

HCG STAT-PAK

K-Number: K923925 · 1992-12-24

Decision Date1992-12-24
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HCG STAT-PAK is the device name listed in this FDA 510(k) record. The listed applicant is Chembio Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1992-12-24 under 510(k) number K923925. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HCG STAT-PAK?

HCG STAT-PAK is a medical device that received FDA 510(k) clearance on 1992-12-24. The listed applicant is Chembio Diagnostic Systems, Inc.. The 510(k) number is K923925.

When did HCG STAT-PAK receive FDA 510(k) clearance?

HCG STAT-PAK received FDA 510(k) clearance on 1992-12-24, under 510(k) number K923925.

Who is the listed applicant for HCG STAT-PAK?

The FDA 510(k) record lists Chembio Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HCG STAT-PAK?

The FDA product code for HCG STAT-PAK is JHI.

Other records listing Chembio 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

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