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 Device, Specimen Collection
510(k) Number K950096
Device Name PINWORM EGG COLLECTOR
Applicant
Evergreen Industries, Inc.
2300 E. 49th St.
P.O. Box 58248
Los Angeles,  CA  90059 -0248
Applicant Contact JOHNSON N S. WONG
Correspondent
Evergreen Industries, Inc.
2300 E. 49th St.
P.O. Box 58248
Los Angeles,  CA  90059 -0248
Correspondent Contact JOHNSON N S. WONG
Regulation Number866.2900
Classification Product Code
LIO  
Date Received01/10/1995
Decision Date 04/05/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-