KENDALL BLUNT TUOHY EPIDURAL NEEDLE


Device Classification Name

anesthesia conduction kit

510(k) Number K954706
Device Name KENDALL BLUNT TUOHY EPIDURAL NEEDLE
Applicant
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
15 hampshire st.
mansfield, 
MA 
02048

Applicant Contact david a olson
Correspondent
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
15 hampshire st.
mansfield, 
MA 
02048

Correspodent Contact david a olson
Regulation Number 868.5140
Classification Product Code
CAZ  
Date Received 10/12/1995
Decision Date 05/30/1996
Decision

substantially equivalent – with drug

(SESD)

Regulation Medical Specialty

Anesthesiology

510k Review Panel

Anesthesiology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No