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, Aspiration And Injection, Disposable
510(k) Number K860582
Device Name TBI NEEDLE
Applicant
Hobbs Medical, Inc.
P.O. Box 46
Spring St.
Stafford Springs,  CT  06076
Applicant Contact STEVEN G RICHTER
Correspondent
Hobbs Medical, Inc.
P.O. Box 46
Spring St.
Stafford Springs,  CT  06076
Correspondent Contact STEVEN G RICHTER
Regulation Number878.4800
Classification Product Code
GAA  
Date Received02/18/1986
Decision Date 03/04/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
-
-