LFRE INDIRECT LARYNGOSCOPE


Device Classification Name

nasopharyngoscope (flexible or rigid)

510(k) Number K023004
Device Name LFRE INDIRECT LARYNGOSCOPE
Original Applicant
ASTRALITE CORP.
7701 woodley ave.
van nuys, 
CA 
91406

Original Contact dorian swartz
Regulation Number 874.4760
Classification Product Code
EOB  
Date Received 09/09/2002
Decision Date 01/28/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Ear Nose & Throat

510k Review Panel

Ear Nose & Throat

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No