INTERTECH METERED DOSE ELBOW— 510(k) K895144

Substantially Equivalent

Intertech/Ohio

FDA 510(k) clearance K895144 for INTERTECH METERED DOSE ELBOW, Substantially Equivalent on 1989-10-19. Applicant: Intertech/Ohio. Device class: 1.

Clearance details

Applicant: Intertech/Ohio
Product code: Code BZA
Device class: Class 1
Regulation: 21 CFR 868.5810
Advisory panel: Anesthesiology
Date received: 1989-08-18
Decision date: 1989-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Myers, FL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Intertech/Ohio

K890346 — INTERTECH UNIVERSAL HYDROPHOBIC FILTER1989-03-01
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K884526 — ADULT RESUSCITATOR WITH MASK AND FILTER1988-11-16
K882204 — RESUSCITATOR VALVE ASSEMBLY W/FILTER1988-07-08
K880394 — FIRST RESPONSE PEDIATRIC EMERGENCY RESUSCITATOR1988-02-29

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