510(k) K903649

BRADLEY TENACULUM HOLDER by Marlo Surgical Technology — Product Code KDC

K903649 is an FDA 510(k) premarket notification submitted by Marlo Surgical Technology for the device "BRADLEY TENACULUM HOLDER". The FDA issued a decision of Substantially Equivalent on November 2, 1990. The device falls under product code KDC (Instrument, Surgical, Disposable), a Class I device regulated under 21 CFR 878.4800. Marlo Surgical Technology has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 2, 1990
Date Received
August 13, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Surgical, Disposable
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type