510(k) K821024
K821024 is an FDA 510(k) premarket notification submitted by Howmedica Corp. for the device "DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE". The FDA issued a decision of Substantially Equivalent on May 14, 1982. The device falls under product code GDT (Staple, Removable (Skin)), a Class I device regulated under 21 CFR 878.4760. Howmedica Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 14, 1982
- Date Received
- April 13, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Staple, Removable (Skin)
- Device Class
- Class I
- Regulation Number
- 878.4760
- Review Panel
- SU
- Submission Type