INSPIROMETER RESPIRATORY EXERCISER— 510(k) K770141

Substantially Equivalent

Medi, Inc.

FDA 510(k) clearance K770141 for INSPIROMETER RESPIRATORY EXERCISER, Substantially Equivalent on 1977-02-01. Applicant: Medi, Inc.. Device class: 2.

Clearance details

Applicant: Medi, Inc.
Product code: Code BWF
Device class: Class 2
Regulation: 21 CFR 868.5690
Advisory panel: Anesthesiology
Date received: 1977-01-24
Decision date: 1977-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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