510(k) K910764

Device
THE PERCEPTOR(TM) STAND ALONE TRANSDUCER
Applicant
NORTH AMERICAN INSTRUMENT CORP.
510(k) number
K910764
Product code
DRS  
Decision
Substantially Equivalent (SESE)
Decision date
1991-04-22
Date received
1991-01-31
Regulation
870.2850
Classification name
Transducer, Blood-pressure, Extravascular
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Third party reviewed
No
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
ROBERT E FRANKLIN
Address
Glens Falls NY US 12801 12801

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

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Legacy Summary

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FDA Review

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