INSUL-LINE
K-Number: K911443 · 1991-07-26
Advertisement
Device Summary
Frequently Asked Questions
What is the INSUL-LINE?
INSUL-LINE is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Trademark Corp.. The 510(k) number is K911443.
When did INSUL-LINE receive FDA 510(k) clearance?
INSUL-LINE received FDA 510(k) clearance on 1991-07-26, under 510(k) number K911443.
Who is the listed applicant for INSUL-LINE?
The FDA 510(k) record lists Trademark Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INSUL-LINE?
The FDA product code for INSUL-LINE is FPA.
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.
Related Devices (Code: FPA)
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