CA AND ST
K-Number: K926155 · 1994-03-04
Advertisement
Device Summary
Frequently Asked Questions
What is the CA AND ST?
CA AND ST is a medical device that received FDA 510(k) clearance on 1994-03-04. The listed applicant is Dabi-Atlante America Corp.. The 510(k) number is K926155.
When did CA AND ST receive FDA 510(k) clearance?
CA AND ST received FDA 510(k) clearance on 1994-03-04, under 510(k) number K926155.
Who is the listed applicant for CA AND ST?
The FDA 510(k) record lists Dabi-Atlante America Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CA AND ST?
The FDA product code for CA AND ST is EFB.
Other records listing Dabi-Atlante America Corp. 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: EFB)
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.
Advertisement