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FDA 510(k)

KODAK SURECELL(TM) HCG-URINE TEST KIT

K-Number: K902136 · 1990-06-28

Decision Date1990-06-28
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KODAK SURECELL(TM) HCG-URINE TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Eastman Kodak Company. It received FDA 510(k) clearance on 1990-06-28 under 510(k) number K902136. 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 KODAK SURECELL(TM) HCG-URINE TEST KIT?

KODAK SURECELL(TM) HCG-URINE TEST KIT is a medical device that received FDA 510(k) clearance on 1990-06-28. The listed applicant is Eastman Kodak Company. The 510(k) number is K902136.

When did KODAK SURECELL(TM) HCG-URINE TEST KIT receive FDA 510(k) clearance?

KODAK SURECELL(TM) HCG-URINE TEST KIT received FDA 510(k) clearance on 1990-06-28, under 510(k) number K902136.

Who is the listed applicant for KODAK SURECELL(TM) HCG-URINE TEST KIT?

The FDA 510(k) record lists Eastman Kodak Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KODAK SURECELL(TM) HCG-URINE TEST KIT?

The FDA product code for KODAK SURECELL(TM) HCG-URINE TEST KIT 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 Eastman Kodak Company 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.

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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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