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 Source, Carrier, Fiberoptic Light
510(k) Number K932131
Device Name MID LABS TWIN ILLUMINATOR
Applicant
Medical Instrument Development Laboratories, Inc.
2235 Polvorosa Ave.
Suite 200
San Leandro,  CA  94577
Applicant Contact DAVID E CHEN
Correspondent
Medical Instrument Development Laboratories, Inc.
2235 Polvorosa Ave.
Suite 200
San Leandro,  CA  94577
Correspondent Contact DAVID E CHEN
Regulation Number874.4350
Classification Product Code
EQH  
Date Received05/03/1993
Decision Date 04/01/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-