CEFPROZIL 30MCG, SENSI DISC
K-Number: K920473 · 1992-03-23
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Device Summary
Frequently Asked Questions
What is the CEFPROZIL 30MCG, SENSI DISC?
CEFPROZIL 30MCG, SENSI DISC is a medical device that received FDA 510(k) clearance on 1992-03-23. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K920473.
When did CEFPROZIL 30MCG, SENSI DISC receive FDA 510(k) clearance?
CEFPROZIL 30MCG, SENSI DISC received FDA 510(k) clearance on 1992-03-23, under 510(k) number K920473.
Who is the listed applicant for CEFPROZIL 30MCG, SENSI DISC?
The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CEFPROZIL 30MCG, SENSI DISC?
The FDA product code for CEFPROZIL 30MCG, SENSI DISC is JTN.
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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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: JTN)
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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