• 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 Unit, Operative Dental
510(k) Number K895876
Device Name RAMVAC DENTAL VACUUM SYSTEM
Applicant
Ramvac Corp.
120 E. Michigan St.
Spearfish,  SD  57783
Applicant Contact MEYER, DDS
Correspondent
Ramvac Corp.
120 E. Michigan St.
Spearfish,  SD  57783
Correspondent Contact MEYER, DDS
Regulation Number872.6640
Classification Product Code
EIA  
Date Received10/05/1989
Decision Date 12/26/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-