• 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 Calculator, Pulmonary Function Data
510(k) Number K830954
Device Name ACOH WELLNESS TESTER
Applicant
BRADLEY, CAMPBELL & CARNEY
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
BRADLEY, CAMPBELL & CARNEY
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.1880
Classification Product Code
BZC  
Date Received03/25/1983
Decision Date 06/10/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-