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 Reagent & Control, Partial Thromboplastin Time
510(k) Number K880711
Device Name CLP 0.02 M CALCIUM CHLORIDE SOLUTION.
Applicant
CREATIVE LABORATORY PRODUCTS, INC.
6258 LA PAS TRAIL
INDIANAPOLIS,  IN  46268
Applicant Contact ROY SPECK
Correspondent
CREATIVE LABORATORY PRODUCTS, INC.
6258 LA PAS TRAIL
INDIANAPOLIS,  IN  46268
Correspondent Contact ROY SPECK
Regulation Number864.7925
Classification Product Code
GIT  
Date Received02/22/1988
Decision Date 03/18/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-