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FDA 510(k)

ADD'L USES FOR THE KODAK SURECELL CHLAMYDIA KIT

K-Number: K900402 · 1990-03-08

ApplicantEastman Kodak Company
Decision Date1990-03-08
Product CodeLJC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ADD'L USES FOR THE KODAK SURECELL CHLAMYDIA 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 1990-03-08 under 510(k) number K900402. The device is classified under product code LJC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADD'L USES FOR THE KODAK SURECELL CHLAMYDIA KIT?

ADD'L USES FOR THE KODAK SURECELL CHLAMYDIA KIT is a medical device that received FDA 510(k) clearance on 1990-03-08. The listed applicant is Eastman Kodak Company. The 510(k) number is K900402.

When did ADD'L USES FOR THE KODAK SURECELL CHLAMYDIA KIT receive FDA 510(k) clearance?

ADD'L USES FOR THE KODAK SURECELL CHLAMYDIA KIT received FDA 510(k) clearance on 1990-03-08, under 510(k) number K900402.

Who is the listed applicant for ADD'L USES FOR THE KODAK SURECELL CHLAMYDIA 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 ADD'L USES FOR THE KODAK SURECELL CHLAMYDIA KIT?

The FDA product code for ADD'L USES FOR THE KODAK SURECELL CHLAMYDIA KIT is LJC.

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Other records listing Eastman Kodak Company as applicant

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Related Devices (Code: LJC)

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.

K032330CT OIAThermo Biostar, Inc.K033865IDEIA PCE CHLAMYDIADakocytomation, Ltd.K033079CHLAMYDIA IGG ELISA TEST SYSTEMTrinity Biotech USAK982210MODIFICATION OF SYVA MICROTRAK II CHLAMYDIA EIADade Behring, Inc.K962558CHLAMYDIA IGG ELISA TEST SYSTEMArmkel, LLCK960850ACCESS CHLAMYDIA ASSAYBio-Rad Laboratories, Inc.

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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