• 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 K872558
Device Name CART, EMERGENCY, CARDIOPULMONARY
Applicant
Nico Metal Products Corp.
373 Van Sinderen Ave.
Brooklyn,  NY  11207
Applicant Contact NICOLO PRAVATA
Correspondent
Nico Metal Products Corp.
373 Van Sinderen Ave.
Brooklyn,  NY  11207
Correspondent Contact NICOLO PRAVATA
Regulation Number868.6175
Classification Product Code
BZN  
Date Received06/29/1987
Decision Date 07/24/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-