RESPAIDE— 510(k) K980052

Substantially Equivalent

Emergency Filtration Products, Inc.

FDA 510(k) clearance K980052 for RESPAIDE, Substantially Equivalent on 1998-08-05. Applicant: Emergency Filtration Products, Inc.. Device class: 2.

Clearance details

Applicant: Emergency Filtration Products, Inc.
Product code: Code CBP
Device class: Class 2
Regulation: 21 CFR 868.5870
Advisory panel: Anesthesiology
Date received: 1998-01-06
Decision date: 1998-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. George, UT, US

Download summary PDF View on FDA.gov ↗

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