510(k) K894367
K894367 is an FDA 510(k) premarket notification submitted by Beiersdorf, Inc. for the device "LEUKOSPORT(TM) ADHESIVE TAPE". The FDA issued a decision of SN on November 15, 1989. The device falls under product code KGX (Tape And Bandage, Adhesive), a Class I device regulated under 21 CFR 880.5240. Beiersdorf, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- November 15, 1989
- Date Received
- July 14, 1989
- 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