510(k) K930030

SUCTION TUBES: HOUSE, BARON by Thomasville Medical Assoc. — Product Code JCX

K930030 is an FDA 510(k) premarket notification submitted by Thomasville Medical Assoc. for the device "SUCTION TUBES: HOUSE, BARON". The FDA issued a decision of Substantially Equivalent on February 25, 1994. The device falls under product code JCX (Apparatus, Suction, Ward Use, Portable, Ac-Powered), a Class II device regulated under 21 CFR 878.4780. Thomasville Medical Assoc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 25, 1994
Date Received
January 5, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apparatus, Suction, Ward Use, Portable, Ac-Powered
Device Class
Class II
Regulation Number
878.4780
Review Panel
SU
Submission Type