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
510(k) Number K844609
Device Name PERRY SUTURING SET
Applicant
Perry, Div.
1875 Harsh Ave. SE
P.O. Box 550
Massillon,  OH  44648
Applicant Contact JAMES R CHATTERTON
Correspondent
Perry, Div.
1875 Harsh Ave. SE
P.O. Box 550
Massillon,  OH  44648
Correspondent Contact JAMES R CHATTERTON
Date Received11/27/1984
Decision Date 01/15/1985
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-