DESARA SL
K-Number: K121928 · 2013-02-19
Advertisement
Device Summary
Frequently Asked Questions
What is the DESARA SL?
DESARA SL is a medical device that received FDA 510(k) clearance on 2013-02-19. The listed applicant is Caldera Medical, Inc.. The 510(k) number is K121928.
When did DESARA SL receive FDA 510(k) clearance?
DESARA SL received FDA 510(k) clearance on 2013-02-19, under 510(k) number K121928.
Who is the listed applicant for DESARA SL?
The FDA 510(k) record lists Caldera Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DESARA SL?
The FDA product code for DESARA SL is OTN.
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 Caldera 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: OTN)
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