• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BAUSCH AND LOMB FLYING SPOT LASER

  • 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
 

BAUSCH AND LOMB FLYING SPOT LASER Back to Search Results
Event Date 08/22/2007
Event Type  Injury  
Event Description

Developed chronic dry eyes - 8 month beyond prk - flying spot bausch and lomb laser. Never had dry eyes prior to the procedure.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Type of DeviceFLYING SPOT LASER
Manufacturer (Section D)
BAUSCH AND LOMB
MDR Report Key1058377
Report NumberMW5007235
Device Sequence Number1
Product CodeHQF
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 06/06/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received06/06/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Health Professional
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 06/06/2008 Patient Sequence Number: 1
-
-