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FDA 510(k)

K-MESH

K-Number: K843829 · 1985-06-05

ApplicantKatecho, Inc.
Decision Date1985-06-05
Product Code
DecisionSubstantially Equivalent

Device Summary

K-MESH is the device name listed in this FDA 510(k) record. The listed applicant is Katecho, Inc.. It received FDA 510(k) clearance on 1985-06-05 under 510(k) number K843829. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-MESH?

K-MESH is a medical device that received FDA 510(k) clearance on 1985-06-05. The listed applicant is Katecho, Inc.. The 510(k) number is K843829.

When did K-MESH receive FDA 510(k) clearance?

K-MESH received FDA 510(k) clearance on 1985-06-05, under 510(k) number K843829.

Who is the listed applicant for K-MESH?

The FDA 510(k) record lists Katecho, Inc. as the applicant. This does not by itself establish the device manufacturer.

Other records listing Katecho, 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.

K012404K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85K010543KM-30 TENS ELECTRODEK003228K-DEFIB/PACE MULTIFUCTION PEDIATRIC ELECTRODE, MODEL KDP-70AK002806K-DEFIB/PACE, MODEL KDP-60AK000870KM-10 TENS ELECTRODEK993745K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-80

View all 26 devices →

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.

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