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FDA 510(k)

INSUL-LINE

K-Number: K911443 · 1991-07-26

Decision Date1991-07-26
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INSUL-LINE is the device name listed in this FDA 510(k) record. The listed applicant is Trademark Corp.. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K911443. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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