VENTURI PHACO PACK

Device Classification Name

unit, phacofragmentation

510(k) Number K033653
Device Name VENTURI PHACO PACK
Applicant
BAUSCH & LOMB, INC.
3365 tree ct. industrial blvd.
st. louis, 
MO 
63122 -6694

Applicant Contact dennis pozzo
Correspondent
BAUSCH & LOMB, INC.
3365 tree ct. industrial blvd.
st. louis, 
MO 
63122 -6694

Correspodent Contact dennis pozzo
Regulation Number 886.4670
Classification Product Code
HQC  
Date Received 11/21/2003
Decision Date 12/17/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Ophthalmic

510k Review Panel

Ophthalmic

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls