510(k) K861929

PULMONARY FUNCTION TEST LABORATORY, SYSTEM 1070 by Medical Graphics Corp. — Product Code BZM

K861929 is an FDA 510(k) premarket notification submitted by Medical Graphics Corp. for the device "PULMONARY FUNCTION TEST LABORATORY, SYSTEM 1070". The FDA issued a decision of SN on September 26, 1986. The device falls under product code BZM (Calculator, Pulmonary Function Interpretor (Diagnostic)), a Class II device regulated under 21 CFR 868.1900. Medical Graphics Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
September 26, 1986
Date Received
May 20, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calculator, Pulmonary Function Interpretor (Diagnostic)
Device Class
Class II
Regulation Number
868.1900
Review Panel
AN
Submission Type