PORTA-RESP MONITOR— 510(k) K943146

Substantially Equivalent

S & M Instrument Co.

FDA 510(k) clearance K943146 for PORTA-RESP MONITOR, Substantially Equivalent on 1994-11-28. Applicant: S & M Instrument Co.. Device class: 2.

Clearance details

Applicant: S & M Instrument Co.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1994-06-30
Decision date: 1994-11-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Doylestown, PA, 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.