• 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 Transducer, Ultrasonic, Diagnostic
510(k) Number K961757
Device Name ECOGEL 100 ULTRASOUND GEL
Applicant
Eco-Med Pharmaceuticals, Inc.
6155 Tomken Rd.
Unit 13
Mississauga, Ontario,  CA L4W 1H3
Applicant Contact PAUL L HOOEY
Correspondent
Eco-Med Pharmaceuticals, Inc.
6155 Tomken Rd.
Unit 13
Mississauga, Ontario,  CA L4W 1H3
Correspondent Contact PAUL L HOOEY
Regulation Number892.1570
Classification Product Code
ITX  
Date Received05/06/1996
Decision Date 07/25/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
Recalls CDRH Recalls
-
-