• 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 Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
510(k) Number K834558
Device Name CK10000 SERIES POUCH & BAGS ETC.
Applicant
Currie Medical Specialties, Inc.
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Currie Medical Specialties, Inc.
4221 Richmond Rd., NW
Walker,  MI  49534
Regulation Number880.6850
Classification Product Code
KCT  
Date Received12/28/1983
Decision Date 09/05/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-