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 Mask, Surgical
510(k) Number K123115
Device Name ACME SURGICAL FACE MASK WITH EAR-LOOP MODEL YN-501 AB/W/G/P
Applicant
ACME FILTER MASK INC.
NO. 57 HU SHAN ROAD
YINGGE DISTRICT
NEW TAIPEI CITY,  TW 23941
Applicant Contact JEN KE-MIN
Correspondent
ACME FILTER MASK INC.
NO. 57 HU SHAN ROAD
YINGGE DISTRICT
NEW TAIPEI CITY,  TW 23941
Correspondent Contact JEN KE-MIN
Regulation Number878.4040
Classification Product Code
FXX  
Date Received10/03/2012
Decision Date 05/20/2013
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-