510(k) K853796

RAYLOR RETRACTORS by Cedar Surgical, Inc. — Product Code GAD

K853796 is an FDA 510(k) premarket notification submitted by Cedar Surgical, Inc. for the device "RAYLOR RETRACTORS". The FDA issued a decision of Substantially Equivalent on October 7, 1985. The device falls under product code GAD (Retractor), a Class I device regulated under 21 CFR 878.4800. Cedar Surgical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 7, 1985
Date Received
September 11, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Retractor
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type