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 cart, emergency, cardiopulmonary (excluding equipment)
510(k) Number K924373
Device Name ACCUFLATE ACCESSORIE CART W/IV POLE AND CLAMP
Applicant
INSTRUMED, INC.
11818 N. CREEK PARKWAY NORTH
SUITE 105
BOTHELL,  WA  98011
Applicant Contact JERRY L SPENCE
Correspondent
INSTRUMED, INC.
11818 N. CREEK PARKWAY NORTH
SUITE 105
BOTHELL,  WA  98011
Correspondent Contact JERRY L SPENCE
Regulation Number868.6175
Classification Product Code
BZN  
Date Received08/28/1992
Decision Date 11/25/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-