Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name set, tubing and support, ventilator (w harness)
510(k) Number K770354
Device Name TUBING, AEROSAL, DISPOSABLE
Applicant
INHAL-O-TECH MEDICAL PLASTIC
P.O. Box 385
Blue Spring,  MO  64015
Applicant Contact J.W. Brown
Correspondent
INHAL-O-TECH MEDICAL PLASTIC
P.O. Box 385
Blue Spring,  MO  64015
Correspondent Contact J.W. Brown
Regulation Number868.5975
Classification Product Code
BZO  
Date Received02/22/1977
Decision Date 03/16/1977
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-