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FDA 510(k)

SCRIPPS LABORATORIES HCG ONE-STEP

K-Number: K962906 · 1996-08-23

Decision Date1996-08-23
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SCRIPPS LABORATORIES HCG ONE-STEP is the device name listed in this FDA 510(k) record. The listed applicant is Scripps Laboratories, Inc.. It received FDA 510(k) clearance on 1996-08-23 under 510(k) number K962906. 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 SCRIPPS LABORATORIES HCG ONE-STEP?

SCRIPPS LABORATORIES HCG ONE-STEP is a medical device that received FDA 510(k) clearance on 1996-08-23. The listed applicant is Scripps Laboratories, Inc.. The 510(k) number is K962906.

When did SCRIPPS LABORATORIES HCG ONE-STEP receive FDA 510(k) clearance?

SCRIPPS LABORATORIES HCG ONE-STEP received FDA 510(k) clearance on 1996-08-23, under 510(k) number K962906.

Who is the listed applicant for SCRIPPS LABORATORIES HCG ONE-STEP?

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

What is the FDA product code for SCRIPPS LABORATORIES HCG ONE-STEP?

The FDA product code for SCRIPPS LABORATORIES HCG ONE-STEP 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.

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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