LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension
K-Number: K220691 · 2022-05-05
Device Summary
Frequently Asked Questions
What is the LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension?
LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension is a medical device that received FDA 510(k) clearance on 2022-05-05. The listed applicant is Seigla Medical, Inc.. The 510(k) number is K220691.
When did LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension receive FDA 510(k) clearance?
LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension received FDA 510(k) clearance on 2022-05-05, under 510(k) number K220691.
Who is the listed applicant for LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension?
The FDA 510(k) record lists Seigla Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension?
The FDA product code for LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension is DQY.
Other records listing Seigla 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: DQY)
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.