510(k) K761035
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