510(k) K921761
K921761 is an FDA 510(k) premarket notification submitted by Absentee Shawnee Bandage Group for the device "SHAWNEE PRODUCTS KIT II". The FDA issued a decision of Substantially Equivalent (with conditions) on March 18, 1993. The device falls under product code KGX (Tape And Bandage, Adhesive), a Class I device regulated under 21 CFR 880.5240. Absentee Shawnee Bandage Group has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESD (Substantially Equivalent (with conditions))
- Decision Date
- March 18, 1993
- Date Received
- April 14, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tape And Bandage, Adhesive
- Device Class
- Class I
- Regulation Number
- 880.5240
- Review Panel
- SU
- Submission Type