M/L-10 CLIP APPLIER STERILIZATION TRAY (Catalog#3706)
K-Number: K152743 · 2016-02-08
Device Summary
Frequently Asked Questions
What is the M/L-10 CLIP APPLIER STERILIZATION TRAY (Catalog#3706)?
M/L-10 CLIP APPLIER STERILIZATION TRAY (Catalog#3706) is a medical device that received FDA 510(k) clearance on 2016-02-08. The listed applicant is Microline Surgical, Inc.. The 510(k) number is K152743.
When did M/L-10 CLIP APPLIER STERILIZATION TRAY (Catalog#3706) receive FDA 510(k) clearance?
M/L-10 CLIP APPLIER STERILIZATION TRAY (Catalog#3706) received FDA 510(k) clearance on 2016-02-08, under 510(k) number K152743.
Who is the listed applicant for M/L-10 CLIP APPLIER STERILIZATION TRAY (Catalog#3706)?
The FDA 510(k) record lists Microline Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for M/L-10 CLIP APPLIER STERILIZATION TRAY (Catalog#3706)?
The FDA product code for M/L-10 CLIP APPLIER STERILIZATION TRAY (Catalog#3706) is KCT.
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 Microline Surgical, 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: KCT)
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.