GENERAL PROCEDURE KIT


Device Classification Name

syringe, piston

510(k) Number K960248
Device Name GENERAL PROCEDURE KIT
Applicant
PHYSICIAN INDUSTRIES, INC.
101 north 700 wst
p.o. box 540793
north salt lake, 
UT 
84054 -0793

Applicant Contact brian baker
Correspondent
PHYSICIAN INDUSTRIES, INC.
101 north 700 wst
p.o. box 540793
north salt lake, 
UT 
84054 -0793

Correspodent Contact brian baker
Regulation Number 880.5860
Classification Product Code
FMF  
Date Received 01/16/1996
Decision Date 04/12/1996
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

Type Traditional
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls