AIRSTIRRUP PNEUMATIC ANKLE BRACE— 510(k) K780979

Substantially Equivalent

Aircast, Inc.

FDA 510(k) clearance K780979 for AIRSTIRRUP PNEUMATIC ANKLE BRACE, Substantially Equivalent on 1978-06-30. Applicant: Aircast, Inc.. Device class: 1.

Clearance details

Applicant: Aircast, Inc.
Product code: Code IQI
Device class: Class 1
Regulation: 21 CFR 890.3475
Advisory panel: Physical Medicine
Date received: 1978-06-09
Decision date: 1978-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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