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 Plethysmograph, Impedance
510(k) Number K881851
Device Name VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER
Applicant
Micro Medical, Ltd.
Suite 972
200 SW Market
Portland,  OR  97201
Applicant Contact WILLIAM WEINSTEIN
Correspondent
Micro Medical, Ltd.
Suite 972
200 SW Market
Portland,  OR  97201
Correspondent Contact WILLIAM WEINSTEIN
Regulation Number870.2770
Classification Product Code
DSB  
Date Received05/02/1988
Decision Date 09/26/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-