CLINICAL CHEM.ANAL.ACID,PROSTATIC ACID PHOSPHATASE
K-Number: K914167 · 1992-03-17
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Device Summary
Frequently Asked Questions
What is the CLINICAL CHEM.ANAL.ACID,PROSTATIC ACID PHOSPHATASE?
CLINICAL CHEM.ANAL.ACID,PROSTATIC ACID PHOSPHATASE is a medical device that received FDA 510(k) clearance on 1992-03-17. The listed applicant is Eastman Kodak Company. The 510(k) number is K914167.
When did CLINICAL CHEM.ANAL.ACID,PROSTATIC ACID PHOSPHATASE receive FDA 510(k) clearance?
CLINICAL CHEM.ANAL.ACID,PROSTATIC ACID PHOSPHATASE received FDA 510(k) clearance on 1992-03-17, under 510(k) number K914167.
Who is the listed applicant for CLINICAL CHEM.ANAL.ACID,PROSTATIC ACID PHOSPHATASE?
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 CLINICAL CHEM.ANAL.ACID,PROSTATIC ACID PHOSPHATASE?
The FDA product code for CLINICAL CHEM.ANAL.ACID,PROSTATIC ACID PHOSPHATASE is CKE.
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.
Related Devices (Code: CKE)
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
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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