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FDA 510(k)

KODAK SURECELL HCG URINE TEST, MODIFICATION

K-Number: K936287 · 1994-04-08

ApplicantEastman Kodak Company
Decision Date1994-04-08
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KODAK SURECELL HCG URINE TEST, MODIFICATION 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 1994-04-08 under 510(k) number K936287. 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 HCG URINE TEST, MODIFICATION?

KODAK SURECELL HCG URINE TEST, MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-04-08. The listed applicant is Eastman Kodak Company. The 510(k) number is K936287.

When did KODAK SURECELL HCG URINE TEST, MODIFICATION receive FDA 510(k) clearance?

KODAK SURECELL HCG URINE TEST, MODIFICATION received FDA 510(k) clearance on 1994-04-08, under 510(k) number K936287.

Who is the listed applicant for KODAK SURECELL HCG URINE TEST, MODIFICATION?

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 HCG URINE TEST, MODIFICATION?

The FDA product code for KODAK SURECELL HCG URINE TEST, MODIFICATION is JHI.

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Other records listing Eastman Kodak Company as applicant

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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.

K262299Instant-View® hCG Combo II Cassette TestAlfa Scientific Designs, Inc.K241919Innovita HCG Pregnancy Rapid Combo TestInnovita (Tangshan) Biological Technology Co., Ltd.K203272Alltest Pregnancy Rapid Combo Test CassetteHangzhou AllTest Biotech Co., Ltd.K172322Atellica IM Total hCG (ThCG)Siemens Healthcare Diagnostics, Inc.K172257TrueDX hCG Early Result Pregnancy Test (Midstream Format), TrueDX hCG Early Result Pregnancy Test (Cassette Format), VeriClear Early Result Pregnancy Test (Midstream Format), VeriClear Early Result Pregnancy Test (Cassette Format)True Diagnostics, Inc.K152768Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy Serum/Urine Combo Test StripAssure Tech. Co., Ltd.

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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