510(k) K761035

SURGICAL BLADE HANDLES by Parke-Davis Co. — Product Code GDZ

K761035 is an FDA 510(k) premarket notification submitted by Parke-Davis Co. for the device "SURGICAL BLADE HANDLES". The FDA issued a decision of Substantially Equivalent on December 21, 1976. The device falls under product code GDZ (Handle, Scalpel), a Class I device regulated under 21 CFR 878.4800. Parke-Davis Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 21, 1976
Date Received
November 15, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Handle, Scalpel
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type