ENDOTRACHEAL TUBE CHANGER

FDA Premarket Approval P800068

This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.

Pre-market Approval Supplement Details

DeviceENDOTRACHEAL TUBE CHANGER
Generic NameChanger, Tube, Endotracheal
ApplicantINSTRUMENTATION INDUSTRIES, INC.
Date Received1980-11-21
Decision Date1981-07-21
Notice Date1981-08-14
PMAP800068
SupplementS
Product CodeLNZ 
Advisory CommitteeAnesthesiology
Expedited ReviewNo
Combination Product No
Applicant Address INSTRUMENTATION INDUSTRIES, INC. 1211 Streets Run Rd. pittsburg, PA 15236

Supplemental Filings

Supplement NumberDateSupplement Type
P800068Original Filing
S002 1999-09-03 Normal 180 Day Track
S001 1998-06-02 Normal 180 Day Track

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