Sparrow Ascent
K-Number: K230796 · 2023-06-20
Device Summary
Frequently Asked Questions
What is the Sparrow Ascent?
Sparrow Ascent is a medical device that received FDA 510(k) clearance on 2023-06-20. The listed applicant is Spark Biomedical, Inc.. The 510(k) number is K230796.
When did Sparrow Ascent receive FDA 510(k) clearance?
Sparrow Ascent received FDA 510(k) clearance on 2023-06-20, under 510(k) number K230796.
Who is the listed applicant for Sparrow Ascent?
The FDA 510(k) record lists Spark Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sparrow Ascent?
The FDA product code for Sparrow Ascent is PZR.
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 Spark Biomedical, 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: PZR)
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.