• 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 Pump, Portable, Aspiration (Manual Or Powered)
510(k) Number K862751
Device Name USA ASPIRATOR
Applicant
U. S. A. MEDICAL CORP.
1569 W. 2650 S.
SUITE 7
OGDEN,  UT  84401
Applicant Contact TED HILLSTEAD
Correspondent
U. S. A. MEDICAL CORP.
1569 W. 2650 S.
SUITE 7
OGDEN,  UT  84401
Correspondent Contact TED HILLSTEAD
Regulation Number878.4780
Classification Product Code
BTA  
Date Received07/22/1986
Decision Date 08/04/1986
Decision SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS (SN)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-