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 K841489
Device Name NORELCO ELECTRONIC DIGITAL BP METER
Applicant
North American Philips Corp.
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
North American Philips Corp.
4221 Richmond Rd., NW
Walker,  MI  49534
Date Received04/10/1984
Decision Date 04/10/1984
Decision SE - Postmarket Surveillance Required (SESP)
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-