CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE
K-Number: K062592 · 2006-11-29
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Device Summary
Frequently Asked Questions
What is the CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE?
CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE is a medical device that received FDA 510(k) clearance on 2006-11-29. The listed applicant is Smiths Medical MD, Inc.. The 510(k) number is K062592.
When did CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE receive FDA 510(k) clearance?
CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE received FDA 510(k) clearance on 2006-11-29, under 510(k) number K062592.
Who is the listed applicant for CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE?
The FDA 510(k) record lists Smiths Medical MD, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE?
The FDA product code for CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE is FRN.
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 Smiths Medical MD, 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: FRN)
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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