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 Antisera, Fluorescent, All Types, Escherichia Coli
510(k) Number K770801
Device Name MICROBIO. PROD. FLUORESCENT ANTIBODY
Applicant
Pfizer Pharmaceuticals
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Pfizer Pharmaceuticals
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.3255
Classification Product Code
GMY  
Date Received05/02/1977
Decision Date 05/25/1977
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Immunology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-