MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER— 510(k) K903209

Name: FDA 510(k) clearance K903209
Creator: U.S. Food and Drug Administration
Published: 1990-12-21

Substantially Equivalent

Adler Instrument Co.

FDA 510(k) clearance K903209 for MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER, Substantially Equivalent on 1990-12-21. Applicant: Adler Instrument Co.. Device class: 2.

Clearance details

Applicant: Adler Instrument Co.
Product code: Code HES
Device class: Class 2
Regulation: 21 CFR 884.1300
Advisory panel: Obstetrics/Gynecology
Date received: 1990-07-20
Decision date: 1990-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norcross, GA, US

Download summary PDF View on FDA.gov ↗

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