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 Continuous Measurement Thermometer
510(k) Number K914005
Device Name FIBEROPTIC TYMPANIC THERMOMETER, MODEL 6000
Applicant
Daily Medical Products, Inc.
3665 Kearny Villa Rd.
Suite 301
San Diego,  CA  92123
Applicant Contact ALAN SEACORD
Correspondent
Daily Medical Products, Inc.
3665 Kearny Villa Rd.
Suite 301
San Diego,  CA  92123
Correspondent Contact ALAN SEACORD
Regulation Number880.2910
Classification Product Code
FLL  
Date Received09/06/1991
Decision Date 07/30/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-