STOCKINETTE— 510(k) K781944

Substantially Equivalent

Kimberly-Clark Corp.

FDA 510(k) clearance K781944 for STOCKINETTE, Substantially Equivalent on 1978-12-29. Applicant: Kimberly-Clark Corp.. Device class: 2.

Clearance details

Applicant: Kimberly-Clark Corp.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1978-11-21
Decision date: 1978-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.