FDA.report

510(k) K842610

Device
GUIDELINES FOR PEDIATRIC ANESTHESIA
Applicant
CRITICAL CARE MICRO COMPUTING
510(k) number
K842610
Product code
CAC  
Decision
Substantially Equivalent (SESE)
Decision date
1984-10-04
Date received
1984-07-05
Regulation
868.5830
Classification name
Apparatus, Autotransfusion
Medical specialty
Anesthesiology
Review panel
Anesthesiology
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

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers

Source Documents

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

Legacy Summary

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FDA Review

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