AQUA-BLANKET HYPER/HYPOHERMIA BLANKET— 510(k) K890852

Substantially Equivalent

Ati

FDA 510(k) clearance K890852 for AQUA-BLANKET HYPER/HYPOHERMIA BLANKET, Substantially Equivalent on 1989-04-14. Applicant: Ati. Device class: 2.

Clearance details

Applicant: Ati
Product code: Code ILO
Device class: Class 2
Regulation: 21 CFR 890.5720
Advisory panel: Physical Medicine
Date received: 1989-02-21
Decision date: 1989-04-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, 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.