510(k) K852462
K852462 is an FDA 510(k) premarket notification submitted by American White Cross, Inc. for the device "TRICOT ADHESIVE BANDAGE". The FDA issued a decision of Substantially Equivalent on July 26, 1985. The device falls under product code KGX (Tape And Bandage, Adhesive), a Class I device regulated under 21 CFR 880.5240. American White Cross, Inc. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 26, 1985
- Date Received
- June 10, 1985
- 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