SUPPORT PRODUCTS EXAMPLE PROSET CAST— 510(k) K830650

Name: FDA 510(k) clearance K830650
Creator: U.S. Food and Drug Administration
Published: 1983-07-07

Substantially Equivalent

Isopedix Corp.

FDA 510(k) clearance K830650 for SUPPORT PRODUCTS EXAMPLE PROSET CAST, Substantially Equivalent on 1983-07-07. Applicant: Isopedix Corp.. Device class: 1.

Clearance details

Applicant: Isopedix Corp.
Product code: Code ITG
Device class: Class 1
Regulation: 21 CFR 890.3025
Advisory panel: Physical Medicine
Date received: 1983-03-03
Decision date: 1983-07-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K833732 — NON WETTING UNDERCAST PADDING1983-12-12

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