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 Chamber, Hyperbaric
510(k) Number K934164
Device Name MODEL 2500E/2500ER HYPERBARIC CHAMBER
Applicant
SECHRIST INDUSTRIES, INC.
4225 EAST LA PALMA
ANAHEIM,  CA  92807
Applicant Contact Kaoru Lee Adair
Correspondent
SECHRIST INDUSTRIES, INC.
4225 EAST LA PALMA
ANAHEIM,  CA  92807
Correspondent Contact Kaoru Lee Adair
Regulation Number868.5470
Classification Product Code
CBF  
Date Received08/27/1993
Decision Date 06/13/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-