CDI(TM) H/S CUVETTE, MODIFICATION
K-Number: K915265 · 1992-01-15
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Device Summary
Frequently Asked Questions
What is the CDI(TM) H/S CUVETTE, MODIFICATION?
CDI(TM) H/S CUVETTE, MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-01-15. The listed applicant is 3M Company. The 510(k) number is K915265.
When did CDI(TM) H/S CUVETTE, MODIFICATION receive FDA 510(k) clearance?
CDI(TM) H/S CUVETTE, MODIFICATION received FDA 510(k) clearance on 1992-01-15, under 510(k) number K915265.
Who is the listed applicant for CDI(TM) H/S CUVETTE, MODIFICATION?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CDI(TM) H/S CUVETTE, MODIFICATION?
The FDA product code for CDI(TM) H/S CUVETTE, MODIFICATION is DRY.
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 3M 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: DRY)
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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