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 Container, Specimen Mailer And Storage, Sterile
510(k) Number K770071
Device Name PINLOCK CONTAINER
Applicant
Perkins Mfg. Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Perkins Mfg. Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number864.3250
Classification Product Code
KDT  
Date Received01/13/1977
Decision Date 02/24/1977
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Pathology
510k Review Panel Pathology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-