ACETAL
K-Number: K022032 · 2002-08-29
Advertisement
Device Summary
Frequently Asked Questions
What is the ACETAL?
ACETAL is a medical device that received FDA 510(k) clearance on 2002-08-29. The listed applicant is Inovativ, LLC. The 510(k) number is K022032.
When did ACETAL receive FDA 510(k) clearance?
ACETAL received FDA 510(k) clearance on 2002-08-29, under 510(k) number K022032.
Who is the listed applicant for ACETAL?
The FDA 510(k) record lists Inovativ, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACETAL?
The FDA product code for ACETAL is EHP.
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 Inovativ, LLC 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: EHP)
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