REDI-DRAPE— 510(k) K830723

Substantially Equivalent

The Oec Group

FDA 510(k) clearance K830723 for REDI-DRAPE, Substantially Equivalent on 1983-04-12. Applicant: The Oec Group. Device class: 2.

Clearance details

Applicant: The Oec Group
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1983-03-08
Decision date: 1983-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from The Oec Group

K831420 — HIP PROSTHESIS -VARIOUS1983-09-20
K811656 — POWERED WHEELCHAIR1981-06-25

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