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 Caliper
510(k) Number K760521
Device Name TAPE MEASURE
Applicant
Mcgaw Laboratories
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Mcgaw Laboratories
4221 Richmond Rd., NW
Walker,  MI  49534
Regulation Number888.4150
Classification Product Code
KTZ  
Date Received08/26/1976
Decision Date 11/12/1976
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-