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 Needle, Spinal, Short Term
510(k) Number K961324
Device Name GLOBAL MEDICAL PRODUCTS SPINAL,CONICAL TIP (SPROTTLE STYLE), WHITACRE STYLE NEEDLES
Applicant
GLOBAL MEDICAL PRODS, INC.
NO STREET ADDRESS
OAKVILLE ONT.L6L 5K9,  CA
Applicant Contact PETER CLARK
Correspondent
GLOBAL MEDICAL PRODS, INC.
NO STREET ADDRESS
OAKVILLE ONT.L6L 5K9,  CA
Correspondent Contact PETER CLARK
Regulation Number868.5150
Classification Product Code
MIA  
Date Received04/08/1996
Decision Date 07/02/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-