CIDEX PLUS 28 DAY SOLUTION
K-Number: K923744 · 1994-03-29
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Device Summary
Frequently Asked Questions
What is the CIDEX PLUS 28 DAY SOLUTION?
CIDEX PLUS 28 DAY SOLUTION is a medical device that received FDA 510(k) clearance on 1994-03-29. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K923744.
When did CIDEX PLUS 28 DAY SOLUTION receive FDA 510(k) clearance?
CIDEX PLUS 28 DAY SOLUTION received FDA 510(k) clearance on 1994-03-29, under 510(k) number K923744.
Who is the listed applicant for CIDEX PLUS 28 DAY SOLUTION?
The FDA 510(k) record lists Johnson & Johnson Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CIDEX PLUS 28 DAY SOLUTION?
The FDA product code for CIDEX PLUS 28 DAY SOLUTION is LRJ. This falls under the Clinical Lab category.
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 Johnson & Johnson Medical, Inc. 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: LRJ)
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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