• 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 arterial blood sampling kit
510(k) Number K781857
Device Name TRAY, ARTERIAL BLOOD GAS SAMPLING
Applicant
JELCO LABORATORIES
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
JELCO LABORATORIES
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.1100
Classification Product Code
CBT  
Date Received11/06/1978
Decision Date 12/11/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-